Research Nurse Resume Samples
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Research Nurse Resume Samples
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EK
E Kemmer
Elmer
Kemmer
57160 Elmore Club
Chicago
IL
+1 (555) 690 9242
57160 Elmore Club
Chicago
IL
Phone
p
+1 (555) 690 9242
Experience
Experience
New York, NY
Research Nurse
New York, NY
Sporer LLC
New York, NY
Research Nurse
- Collaborate with others in order to make recommendations for developments of established processes and procedures
- Provides feedback to members of the management team in the development of policies and procedures as requested
- Implement and perform quality measures to ensure adherence to established standards
- Perform procedures such as administering medications, measuring skin lesions, preparing patient for surgery and assisting physician in surgeries
- Assists with policy and process development relative to clinical research conduct
- Works closely with clinical research coordinators and data managers to complete case report forms and meet all data entry guidelines
- Provides patient care utilizing the nursing process with an interdisciplinary approach, following established nursing procedures and standards
Chicago, IL
Research Nurse Coordinator
Chicago, IL
Hills-Reichel
Chicago, IL
Research Nurse Coordinator
- Assists with research study design, development of research protocol and research project budget development
- Create and maintain study logs for effective trial management and troubleshoot patient management problems/scheduling conflicts
- Participates in education, research and performance improvement activities
- Performs nursing procedures and treatments as directed by physician or LIP in the treatment and management of patient care
- Assist the Principal Investigator in feasibility and budget assessments for research studies, recommend changes and adjustments as necessary
- Assist in the development of research protocols, case report forms, and case report form completion guidelines
- Assists with research project budget development
present
Detroit, MI
Research Nurse, Senior
Detroit, MI
Buckridge, Bayer and Schinner
present
Detroit, MI
Research Nurse, Senior
present
- Provide direct patient care involving diagnosis and administering medication
- Participate in protocol development by reviewing potential protocols, informed consent documents, and evaluate their effect on standard nursing procedures
- Assist physician and/or principal investigator in writing manuscripts for publication and/or presentation of materials at conferences
- Provide training to other staff members to assure patient safety and adherence to the protocol
- Participates in free hepatitis C antibody screening clinic
- Assists physician and/or principal investigator in writing manuscripts for publication and/or presentation of materials at conferences
- Prepares financial records including quarterly reports, budget and patient related expenses
Education
Education
Bachelor’s Degree in Nursing
Bachelor’s Degree in Nursing
University of Virginia
Bachelor’s Degree in Nursing
Skills
Skills
- Ability to communicate conceptually detailed and complex information effectively and professionally with a wide range of people
- The individual is expected to be highly organized, keep detailed records, and display good verbal, communication, and problem-solving skills
- Good computer skills, including working knowledge of a personal computer and Microsoft Office (Word, Access, Excel, and PowerPoint) and basic statistics
- Able to demonstrate professional knowledge within wound prevention and wound treatment to give advice and guidance to internal and external customers
- Ability to implement good clinical practices in all interactions with study participants, their families, and colleagues
- Experience in Asthma/COPD strongly desirable
- Ability to work independently and be an excellent team player
- Experience in RAVE EDC System strongly desirable
- Knowledge of and appropriate application of the nursing process, professional theory, practice and procedures
- Analytical ability to solve clinical nursing issues and conduct quality improvement research utilization projects
15 Research Nurse resume templates
Read our complete resume writing guides
1
Research Nurse Resume Examples & Samples
- 3-5 years of experiences an RN
- 1 year of research experience
- Previous oncology experience
2
Research Nurse Resume Examples & Samples
- Schedule appointments with social workers from Adult Protective Services
- Interview and evaluate older adults – some who have been physically abused – with a standardized instrument
- Complete evaluation forms
- Answer general questions; obtain consent for patient to be involved in study
- Keep meticulous records
- Establish and maintain hard copy and/or electronic files and records
- Photograph injuries and maintain photographs
- Creates and maintains charts, graphs, spreadsheets and databases on a personal computer
- Read and prioritize incoming mail. Handles or routes as appropriate
- Provides assistance in the day-to-day administration of the grant
3
Research Nurse Resume Examples & Samples
- Prepare project approval forms necessary for submission to appropriate committees; design informed consent forms
- Recruitment and enrollment of participants for medical studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met
- Evaluate potential study participants to ensure they meet eligibility requirements; instruct study participants concerning research protocol and complete the patient informed consent procedure
- Schedule and/or perform medical testing such as drawing blood, taking blood pressure reading, performing EKGs, etc. Includes processing and packaging of laboratory samples for shipment
- Assess participants during clinic visit, determining if patient is experiencing side effects or other problems; notify principal investigator if problems arise
- Inventory and requisition supplies and equipment; arrange for repair and maintenance of equipment
- Complete case report forms for each study participant and document medical data in the patient record
- Develop source documents and other data collection/tracking tools as needed
- Minimum of (2) two years clinical research experience
- Cardiovascular or Intensive Care nursing experience
- Detail orientated with solid communication skills
- Demonstrated ability to work autonomously
- CITI training
4
Research Nurse, Senior Resume Examples & Samples
- Supervise Research Nurses/Research staff, when assigned
- Participate in protocol development by drafting study protocols and/or reviewing potential protocols to evaluate their effect on standard nursing procedures; submit to Human Subjects Committee for approval
- Prepare project approval forms necessary for submission to the IRB, site review authority, other committees, and designs informed consent forms
- Recruit study participants by referrals or by placing advertisements on television, radio or in newspapers; schedule appointments, interview and evaluate potential participants to ensure they meet eligibility requirements; instruct participants concerning protocol and obtains consent signature
- Provide direct patient care involving nursing diagnosis, administering medication and performing tests such as pulmonary function, electrocardiograms and allergy tests
- Coordinate and/or perform physical assessments required by protocol such as tumor measurements, neurological checks and blood pressure reading
- Evaluate and develop patient educational materials, and give patient and/or family members instructions on drug administration and other medical information
- Train, oversee and provide current patient information to nurses and other health care and research personnel in order to assure comprehensive patient care
- Complete case report forms for each study participant and document medical data in patient record
- Assess participants for evidence of drug toxicity, unexpected side effects or other problems and notify principal investigator; recommend dosage adjustments
- Assist physician and/or principal investigator in writing manuscripts for publication and/or presentation of materials at conferences
- ACRP or SoCRA certification
- Knowledge of diabetes care
- Experienced in working with patients with chronic illness
5
Research Nurse Resume Examples & Samples
- Teach a wide variety of health education classes (including skills training and health promotion services) in classroom and individual settings to adults with serious mental illnesses to help them improve their health and wellness
- Assist in marketing and outreach recruitment efforts, including presentations to medical providers and participation in community outreach events
- Complete required documentation in compliance with CSA certification, Cenpatico, and ADHS/DBHS requirements, such as progress notes, monthly summaries, incident reports, etc
- Maintain Community Service Agency certification requirements, such as staff credentials, fire codes, recertification of agency through ADHS/DBHS, AHCCCS re-enrollment, etc
- Perform physical assessments such as height, weight, blood pressure, waist circumference, cardiovascular endurance, etc
- Administer basic first aid to HWC program participants
- Conduct staff trainings relating to emergency protocols, fire drills, etc
- Maintain inventory of first aid office supplies
- Work within protocols to maintain a clean, recovery-oriented environment
- Current TB clearance (within the past year) and up-to-date CPR & First Aid certification
- Two or more years of professional experience working with people with serious mental illness or both serious mental illness and substance use disorders
- Knowledge of recovery skills and practices related to supporting people with serious mental illnesses and/or co-occurring substance use disorders
- Knowledge and skills related to stages of change and motivational interviewing
- Ability to inspire people to change their way of thinking, behaving, and replace habits that do not support their health and wellness with new habits and routines that do support
- Comfortable teaching in large class settings as well as one-on-one
- Comfortable documenting services using an electronic medical record system
- Comfortable organizing and maintaining credentialing requirements for the program
- Fluent in Spanish
6
Research Nurse, Senior Resume Examples & Samples
- Participate in protocol development by reviewing potential protocols, informed consent documents, and evaluate their effect on standard nursing procedures
- Provide direct patient care involving diagnosis and administering medication
- Actively participate in disease team meetings
- Develop flowsheets and forms needed to capture specific protocol required data
- Provide training to other staff members to assure patient safety and adherence to the protocol
- Perform lab draws and give injections where an RN license is required
- Other pertinent duties as assigned
- Previous work as an oncology research nurse
- Previous work with the EPIC electronic health record system
- Demonstrated detailed documentation skills
- Demonstrated strong interpersonal, communication, and problem-solving skills
7
Pediatric Research Nurse Resume Examples & Samples
- Minimum of 1 year in a Pediatric setting
- Phlebotomy skills - must be comfortable working with infants
- Ability to pay close attention to study details and strictly follow IRB/FDA regulations
- Ability to work as a member of a team
- Ability to interact in a professional manner with clinical research subjects and other health professionals
- Experience in clinical research
- Experience in operating laboratory equipment and processing specimens
- Prior experience with Electronic Medical Records, specifically EPIC
- Ability to speak Spanish
- A current Resume/CV
- The names, addresses, daytime telephone numbers and e-mail addresses for three professional references, either attached to your resume/CV or uploaded as a separate document
8
Research Nurse Resume Examples & Samples
- Provides nursing care and oversight of clinical trial subjects while complying with Good Clinical Practice, regulatory and protocol requirements
- Communicates subject and/or trial-related information, updates and concerns to Investigators, operational leaders, Project Managers, Project Coordinators, as necessary
- Maintains knowledge of research protocols and attends education sessions provided to research staff involved in conducting trial procedures
- Records study data and maintain source documentation according to Good Documentation Practices
- Knows, understands, and follows teammate guidelines, employment policies, and department or company procedures
- Completes other projects/tasks assigned by management
- Provides consistent, regular, punctual attendance as scheduled
- If LPN-LVN, current license in state of practice required
- If RN, nursing degree from accredited school of nursing required along with current RN license in state of practice
- Minimum one year clinical nursing experience preferred
- Minimum one year dialysis experience required
- Minimum one year research experience preferred
- Able to work evening/night/weekend shifts as necessary to support study schedules
- Deals with confidential information and/or issues using discretion and judgment
9
Research Nurse Resume Examples & Samples
- Performs nursing procedures and treatments as directed by physician or LIP in the treatment and management of patient care
- Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols
- Assists with the development of training and educational material for assigned research protocols
- Provides and documents education as needed
- Assists with research project budget development
- Demonstrates basic computer proficiency
10
Pediatric Research Nurse Resume Examples & Samples
- Bachelors Degree in nursing
- Current and valid RN Colorado licensure
- Previous clinical research
- 3 years of relevant experience, with at least 2 years of pediatric nursing experience, including phlebotomy on infants
- Experience using computer software applications such as Microsoft Excel, Word, and PowerPoint
- Strong interpersonal and communication skills (oral and written)
- Ability to understand complex organizations
- Ability to work independently, within a strong team environment
- Ability to manage multiple responsibilities, often under time pressures
- Attention to detail a must as well as ability to accurately prioritize workflow
- Ability to do home visits for subjects unable to attend hospital/clinics
- Experience with multi-center trials
- Spanish speaking
- Experience with electronic medical records (i.e. EPIC)
- Experience with Access database
- Experience using statistical software
11
Research Nurse, Accrual Site Coordinator Resume Examples & Samples
- Must possess a degree or diploma from a professional nursing program approved by a legally designated State accrediting agency at the time the program was completed
- A minimum of 6 months nursing and/or related clinical research experience
- Knowledge of clinical research data collection and clinical data report preparation
- Experience in the coordination, implementation, and execution of clinical trials
- Experience in a clinical trials outpatient setting
12
Research Nurse Resume Examples & Samples
- Reviews new protocols and other materials provided by study sponsors and gives input to Principal Investigator and Manager, as applicable, regarding Nursing and Research issues in order to determine financial and clinical feasibility
- Coordinates implementation of various protocols for assigned Research projects with appropriate departments throughout Baylor Health Care System (BHCS) by interacting with Principal Investigators and Clinical Managers/Supervisors, providing in-service education for healthcare professionals and working with Pharmacy to ensure a smooth project flow
- Assists with preparation of Institutional Review Board (IRB) materials related to initial review and approval of the study
- Maintains communication with study sponsor and/or designee throughout study
- Assists in maintaining regulatory binders
- Helps ensures applicable study supplies, including study drug and/or devices, are received prior to study initiation
- Develops, field tests and critiques data collection forms and offers suggestions for revisions
- Develops appropriate protocol information sheets and pre-printed Physician Order sets for new investigational drug protocols and revises as indicated throughout the study period. Seeks multidisciplinary input in developing order sets
- Screens patients for eligibility on assigned clinical trials in accordance with HIPAA standards
- 2 Coordinates Research subject consent and entry into appropriate Research studies ensuring that all inclusion and exclusion criteria are met
- Manages Research subjects on assigned clinical trials, which may include the following: scheduling protocol required study visits, ensuring that all protocol required testing and treatments are done per protocol, assessing patients for adverse events, drawing pharmacokinetic and other research samples, and coordinating patient follow-up. Participates in daily clinic operations (Physician Offices and Inpatient Units where trials are being conducted) to include clinical assessment,education and delivery of patient care. May include administering investigational drugs
- Assumes technical responsibility for specific tasks, such as obtaining blood samples by phlebotomy, from arterial lines or central venous catheters in compliance with Baylor standards, centrifuging, specimen preparation, shipping and other related procedures
- 5 Reports serious adverse events (SAEs) in a timely manner per study sponsor (or designee) and IRB requirements
- Assists with regulatory compliance including assisting with preparing IRB materials for approval of protocol amendments, submitting IND Safety Reports to the IRB, completing IRB continuing review reports and assisting with drug accountability
- Accurately completes case report forms in a timely manner
- Completes all applicable Research billing compliance procedures
- Coordinates study-monitoring visits
- 10 Submits completed invoices for applicable patient care charges covered by funded Research studies to Baylor Research Institute (BRI) on a monthly basis
- Helps ensure that all study related activities are complete including returning supplies, returning unused stock of study drug/devices, and confirming that all queries are complete
- Assists with preparing Institutional Review Board final report
- Helps ensure that all study documents are complete and that records are retained per federal, state and institutional standards
- 4 Participates in data analysis and writing and submitting manuscripts and abstracts for publication as appropriate
- 1 Maintains current knowledge of departmental functions through reading literature, attending workshops, seminars and conferences, and by participating in professional organizations
- 2 Utilizes Study Manager Clinical Trials Management System per departmental requirements
- 3Develops, implements and administers Research Nurse policies and procedures
- Conducts audits of Research studies to check the accuracy, integrity and consistency of Research studies
- Cooperates with conduct of BRI quality audits
- Maintains patient and study confidentiality at all times
- Engages in positive working relationship with members of Clinical Trial Research Teams
- 1 Year of Clinical Research Experience
13
Research Nurse Coordinator Resume Examples & Samples
- Assist in prospective collection of data on intubated patients for the purpose to be entered into the NEAR registry
- Observe all intubations to capture as much of the following information pertaining to the intubation as possible using the hard‐copy data collection form
- Retrieve the patient medical record number in StudyTRAX to retrospectively identify and input missing data from the patient’s Emergency Department (AHLTA) chart
- Record treatment and procedures rendered, and observe effects
- Maintain patient medical records; prepare and submit administrative reports
- Participate in in‐service training and continuing education programs for new procedures, techniques and equipment
- Provide clinical support to professional staff at assigned Military Treatment Facilities (MTF)
- Bachelor’s Degree in Nursing or related field required
- Required Certifications: Valid and current professional certifications and licenses required for practice in field
- 5 years of clinical work in specialties such as adult medical critical care, surgery critical care (general, trauma/vascular) or emergency medicine
- Skilled with use of computers and knowledge of Microsoft Office software tools and Adobe Acrobat
- Ability to work effectively and diplomatically in a multidisciplinary team environment interacting and collaborating with a wide range of individuals
14
Research Nurse Resume Examples & Samples
- Current registered nurse (RN) license; contract research organization or relevant experience preferred
- Demonstrated ability to prioritize and organize workload
- Demonstrated knowledge of Good Clinical Practices (GCPs)
- Ability to communicate verbally and in writing at all levels inside and outside the organization
- Basic familiarity with Microsoft Office Suite
- Computer skills, commensurate with Essential Functions, including the ability to learn a validated
15
Research Nurse Coordinator Resume Examples & Samples
- Performs telephone triage
- Participates in education, research and performance improvement activities
- Assists with preparation for audits and response to audits
- Assists with the development of training and educational material for assigned research protocols. Provides and documents education as needed
16
Research Nurse, Phase, Clinical Research Resume Examples & Samples
- Coordinate and participate in clinical research studies conducted by a supervising investigator to ensure that data collected on study volunteers adhere to study protocol; may assist in screening volunteers for inclusion in study based on pre-determined criteria
- Administer investigational drug to volunteers according to study protocol
- Record volunteer clinical data in case report forms (CRFs). Collaborate closely with study investigator informing on relevant adverse events and serious adverse events according to procedures outlined in the protocol
- Excellent skill in attention to detail, planning and organization
17
Oncology Research Nurse Resume Examples & Samples
- Clinical Research Coordination
- Review & lead the development & implementation of Clinical Research undertaken w/in the department
- Maintaining an accurate account of the status of the projects & to regularly update the department on the status
- To drive & encourage the participation in original research carried out in the department
- To establish & maintain good channels of communication w/ other departments w/in the Medical Center, other Medical Centers, non-commercial bodies & pharmaceutical sponsors
- In conjunction w/ or in the absence of, the Department Manager, monitors & plans in advance workload of the department ensuring it is adequately resourced
- Clinical Service & Professional Responsibilities: to work as part of the multidisciplinary team & contribute to the ongoing development of the department
- Minimum three (3) years registered nursing experience
- Bachelor's degree in nursing or related field preferred
- CCRC or CCRP preferred
- Oncology experience a must
- Clinical Trials experience a plus
18
Research Nurse Coordinator Resume Examples & Samples
- Develops procedures and interprets policy
- Assures that all studies are conducted in accordance with regulations established by KFHP, State, and other regulatory bodies
- Recruits and selects new clinical research staff
- Orients new research staff
- Counsels and disciplines staff members who are non-compliance with applicable policies, procedures and standards
- Develops and implements clinical staff training and professional development programs
- Prepares research grants for submission and provides annual reports for CRC and IRB
- Monitors and reviews research study budget throughout fiscal year
- Maintains communications, coordinates and conducts site visits with study sponsors
- Conducts regular staff meetings with research staff
- Assures the proper documentation of all patient visits, site visits, meetings
- Assures that strict adherence to protocol inclusion and exclusion criteria is maintained
- Participates in research data management
- Coordinates research patient recruitment
- Monitor for and assures that appropriate action is taken for patients exhibiting adverse reactions during course of research study
- Provides nursing support of clinical studies as needed
- Develops protocol, analysis and compilation of study results, teaching, publication, and other professional activities
- Minimum one (1) year of adult medical nursing, clinical research, clinical management experience
19
Experienced Research Nurse Resume Examples & Samples
- Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements, including timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of serious adverse events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines
- Serves as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions
- Assesses research subject; completes nursing assessment, documenting findings in research subject records and notifies physician of abnormal findings
- Evaluates, initiates and maintains standards of care consistent with policies and procedures
- Assists with specialized patient care equipment as required by the clinical research protocol
- Administers medications and treatments as ordered by a physician or LIP
- Directs, coordinates and participates in the evaluation and supervision of nursing care provided to research subjects, establishing patient care priorities and delegating nursing activities according to the patient needs and staff qualifications and capabilities
- Conducts and documents the informed consent process
- Minimum three years clinical experience including one year of research experience
- Must have strong organizational, communication and interpersonal skills
- Maintains current knowledge in specialty area
20
Research Nurse Resume Examples & Samples
- Assesses and ensures subject safety during trial
- Proposes and negotiates alternatives for protocol. Educates staff about the scientific aspects of the study
- Applies pharmacological knowledge to help PI determine idiosyncrasies and unexpected results. Evaluates adverse events (AE), intervenes when necessary and reports details to PI. Conducts follow-up to determine resolution of AE. Reports serious AEs to IRB and sponsor
- Presents related information to community for recruitment purposes or to other research professionals in a variety of settings
- Mentors and trains new and subordinate employees
- Helps determine personnel required to complete trial and develop the timeline for trial completion. Reviews study related data to assure compliance with study protocol
- Prepares emergency use report
- Manages pharmacokinetic collection and storage
- Relates lab results to PI and sponsor
- Ensures appropriate maintenance and calibration of equipment
- May perform bedside care
21
Research Nurse Resume Examples & Samples
- Successfully learn how to annotate and abstract using specific tools and methodologies
- Review (and adhere to) guidelines for each project; communicate with managers as warranted
- Effectively and efficiently search for medical concepts within medical notes, (e.g. identify diseases, symptoms, medications, tests, and relationships, as well as indicate the clinical reasoning that takes place given a use case)
- Work independently to meet deadlines for both project-specific and non-project tasks
- Implement and perform quality measures to ensure adherence to established standards
- Obtain HIPAA, IRB CITI course training certifications, and all other required training certifications. Maintain ongoing training certifications as required
- This position has no responsibility for providing care to patients
22
Clinical Trials Research Nurse Resume Examples & Samples
- Compliance: Support & comply w/the Principles of Responsibility (KP Code of Conduct). W/ guidance from PI, assist w/ ensuring compliance w/KPNC IRB approved protocols
- Study Implementation: W/guidance from PI, utilize nursing skills to coordinate research-related activities (e.g., scheduling study visits, assisting w/nursing assessment of participants, adverse events, & data collection including laboratory & diagnostic studies)
- W/ supervision, utilize & Doc the nursing procedures to plan, deliver, & evaluate research care for non-complex medical conditions &, w/appropriate assistance, for complex medical conditions
- W/direction, abstract data from source documentation onto case report forms (paper or electronic) in a timely manner
- Assist w/study completion, resolution of data queries, data lock, study closeout, & archiving of study files
23
Clinical Trial Research Nurse Resume Examples & Samples
- Adhere to Guideline for Good Clinical Practice (GCP), federal, state & local regulations, & KP policies & procedures. W/direction, assist w/any internal/external compliance monitoring &/or audits & inspections to protect research participants, assure operational effectiveness of the program, & to reduce risks to the organization
- Assist in the determination of eligibility of candidates for study participation
- Assist in the identification & procurement of equipment & supplies needed to fulfill protocol requirements
- Accurately & completely record info in source Docs in a timely manner
- W/in the nursing scope of practice, assist the PI w/the care & evaluation of research participants
- Support the effective financial management of the clinical trial
- Minimum two (2) years of clinical nursing experience in a hospital, clinic or similar health care setting within the last three (3) years required (Bachelor's degree may be substituted for one (1) year work experience)
- Minimum of 2-3 years experience as a RN with 1 of the last 2-3 years in oncology required
- Previous research experience desirable but not required
- Ability to make and complete accurate patient assessments
- Demonstrated ability to work independently and cooperatively in multiple settings
- Must be flexible, organized, detail oriented and tenacious in follow-through
- Must possess the ability to work well under pressure
- Must be willing and able to travel
24
Research Nurse Resume Examples & Samples
- Perform all required nursing processes and procedures concomitant with the research protocol
- Administer medication per protocol and medical standards
- Observe and monitor the physical and mental status of study participants throughout study visit
- Communicate in a timely manner to study team all notable participant issues
- Ensure all delegated responsibilities are completed accurately and in a timely manner
- Obtain vital signs, lab specimens (blood and urine), and EKGs when necessary
- Maintain confidentiality for study participants at all times
- Utilize universal precautions in any potential contact with study participant body fluids or used participant supplies that may be contaminated with participant body fluids
- Understanding of research terminology, biology, and knowledge of Good Clinical Practices as demonstrated by prior job experience
- Experience in pharmaceutical sponsored and investigator initiated clinical research trials
- Demonstrated ability to maintain multiple research trials and large study population demands effectively and independently of others
25
Research Nurse, Bone Marrow Transplantation Resume Examples & Samples
- To assess & evaluate the progress of on-going clinical trials & research undertaken in the unit
- To safeguard interest of patients by liaison w/ relevant trial personnel & contribution to trial design & protocol & ensure compliance w/ ICH GCP Guidelines
- To ensure that all proposed research projects carried out in the department are reviewed by the Institutional Review Committee (IRB) prior to commencement & that updates & amendments are reported in a timely fashion
- To provide advice & support to other members of the multidisciplinary team w/ regard to ICH & GCP, project development, implementation, completion & dissemination
- Liaison w/ pharmaceutical sponsors regarding feasibility & implementation aspects of proposed clinical trials
- Liaison w/ the multidisciplinary team to promote & oversee the appropriate referral & recruitment of patients to research w/in the unit for which the post holder has a designated responsibility
- Ensure that all ICH GCP required documentation is kept in a clearly trackable system & is stored in for the appropriate time at all times to ensure clear, accurate records, developing data collection, case report forms & design of database where required
- To establish & maintain good working relationships w/ supporting clinical services
- In conjunction w/ the lead clinician and/or Department Manager develops & updates a strategy for clinical research w/in the department
- Develop standards for research practice & ensure these are reviewed & updated on a regular basis
- Also to review other relevant departmental standards to ensure they are applied appropriately
- Administrative or clinical research experience preferred
26
Research Nurse, Senior Resume Examples & Samples
- Supervises Research Nurses and support staff when assigned
- Participates in protocol development by drafting study protocols and/or reviewing potential protocols to evaluate their effect on standard nursing procedures; submits to Human Subjects Committee and adjacent hospital for approval
- Prepares project approval forms and other necessary regulatory documents necessary for submission to appropriate committees
- Designs informed consent forms and case report forms
- Recruits study participants by referrals or by placing advertisements on television, radio or in newspapers
- Schedules appointments, interviews and evaluates potential study participants to ensure they meet eligibility requirements
- Instructs study participants concerning protocol and obtains consent signature to complete the informed consent process
- Schedules and/or coordinates the scheduling of required laboratory tests and/or exams within the hospital system or with outside providers
- Provides direct patient care involving diagnosis, administering medication, patient teaching and performing tests such as pulmonary function, electrocardiograms and allergy tests
- Coordinates and/or performs physical assessments required by protocol such as tumor measurements, neurological checks and blood pressure reading
- Evaluates and develops patient educational materials and gives patient and/or family members instructions on drug administration and other medical information
- Trains, oversees and provides current patient information to nurses and other health care personnel in order to assure comprehensive patient care
- Completes case report forms and electronic data entry for each study participant and documents medical data in patient record
- Prepares financial records including quarterly reports, budget and patient related expenses
- Assesses participants for evidence of drug toxicity, unexpected side effects or other problems and notifies principal investigator; recommends dosage adjustments
- Assists physician and/or principal investigator in writing manuscripts for publication and/or presentation of materials at conferences
- Inventories and requisitions supplies and equipment; arranges for repair and maintenance of equipment
- Participates in Investigator meetings (In/Out of state)
- Participates in on/off site community health fairs
- Participates in free hepatitis C antibody screening clinic
27
Research Nurse Resume Examples & Samples
- Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements, timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of Serious Adverse Events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines
- Directs, coordinates and participates in the evaluation and supervision of nursing care provided to research subjects; establishing patient care priorities and delegating nursing activities according to the patient needs and staff qualifications and capabilities
- Assists with research study design, development of research protocol and research project budget development
- Minimum five years clinical experience, clinical research experience preferred
28
PRN Research Nurse, Phase, Clinical Research Resume Examples & Samples
- Confer with volunteers to explain purpose of study and obtain informed consent forms; explain procedures and practical issues such as timelines for visits and restrictions on food and drink
- Review CRFs; evaluate and interpret collected data and prepare protocol summary forms, statistical reports and analyses documenting progress, adverse trends and appropriate recommendations or conclusions
- Cooperate with study monitor and reserve sufficient time for questions during monitoring
- Bachelor's degree or educational equivalent in Nursing and 1+ year relevant experience; or equivalent combination of education, training and experience
- Kansas state licensure as an RN
- Telemetry experience preferred
- Experience in training staff members a plus
29
Clinical Trials Research Nurse Resume Examples & Samples
- Oncology certified nurse preferred
- Phlebotomy skills a plus
- Computer skills in WORD, Excel and internet preferred
30
Research Nurse Resume Examples & Samples
- Review (and adhere to) guidelines and protocols for each project; communicate with clinical staff, program manager and research investigators as warranted
- Maintain appropriate documentation and assist research teams in adhering to study timelines
- This position has no responsibility for providing care to patients. This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job
31
Research Nurse Coordinator Resume Examples & Samples
- Establishes a care plan in collaboration with the research subject, family and research team. Coordinates ongoing care
- Maintains professional relationships, using frequent and open effective communication with internal and external constituents
- Minimum three years clinical experience
- Must be self-directed with demonstrated ability to work independently yet establish cooperative relationships with colleagues
- Meets clinical competency requirements
- Participates in process improvement activities
32
Research Nurse Resume Examples & Samples
- Bilingual skills in Spanish
- Minimum 1 year of experience in Clinical Research
- Adult and pediatric phlebotomy training
- Vaccination experience
33
Research Nurse / Clinic Manager Resume Examples & Samples
- Ability to implement study protocols with minimal supervision
- Demonstrated experience with electronic data capture, including database management
- Demonstrated ability to perform the functions of the position with minimal supervision
34
Research Nurse, Senior Resume Examples & Samples
- Supervise Research Nurses and other staff when assigned
- Participate in protocol development by drafting study protocols and/or reviewing potential protocols to evaluate their effect on standard nursing procedures; submit to Human Subjects Committee and Scientific Review Committee for approval
- Recruit study participants by referrals or by placing advertisements on television, radio or in newspapers; schedule appointments, interviews and evaluate potential participants to ensure they meet eligibility requirements; instruct participants concerning protocol and obtain consent signature
- Train, oversee and provide current patient information to nurses and other health care personnel in order to assure comprehensive patient care
- Prepare financial records including quarterly reports, budget and patient related expenses. Maintain close communication with the assigned finance officer for each specific project
- Assist physician and/or principal investigator in writing manuscripts for publication and/or presentation of materials at conferences. Assist in the preparation of NIH, NCI, and PPG grants
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Research Nurse Resume Examples & Samples
- The following duties and responsibilities generally reflect the expectations of this position but are not intended to be all-inclusive
- Provide nursing care and oversight for clinical trial patients to ensure appropriate care for subjects and that trial requirements are met
- Communicate subject or trial procedure information to the Research Unit Supervisor, Charge Nurse, Investigator, and/or Project Manager on an ongoing basis to ensure the safety and integrity of subjects and to ensure data collected for trials
- Ensure compliance with Good Clinical Practice (GCP), regulatory, and protocol requirements
- Perform and maintain source documentation, data collection, drug accountability, Adverse Event (AE) reporting, lab specimen collection, and lab processing for all
- Establish and maintain positive external relationships with dialysis centers and other research partners to ensure effective communications and a streamlined process during trials
- Maintain current awareness and knowledge of research protocols; attend education sessions provided to research staff on trial conduction or research projects
- Assist in recruiting existing subjects for future trials to ensure study timelines are met
- Other duties and responsibilities as assigned including but not limited to
- Work overtime or different shifts as needed
- Provide on-call coverage as needed
- Attend team meetings, phone conferences, and training as needed
- Meet all annual competency and skills tests/checklists as applicable
- Know facility emergency plans and demonstrate ability to act swiftly, confidently in an emergency
- Know, understand, and follow teammate guidelines, employment policies, and department or company procedures
- Consistent, regular, punctual attendance as scheduled is an essential responsibility of this position
- A.D.N degree from accredited school of nursing required; B.S.N preferred; three-year diploma from accredited diploma program may be substituted for nursing degree
- Current RN license in state of practice required
- Hemo-Dialysis Required
- Minimum of one (1) year’s clinical nursing experience strongly preferred
- Electrocardiogram experience preferred
- Phlebotomy skills preferred
- Basic computer skills and proficiency in MS Word Outlook required
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Research Nurse Resume Examples & Samples
- Hospital Systems Knowledge:The ability to track down information through various sources such as medical records, surgery clinics, social security death index, direct patient contact, accounts payable, and legal counsel. The candidate should have some experience gathering
- Data Collection and Reporting
- Identifies surgical patients for inclusion in the program through the application of program inclusion/exclusion criteria and protocols
- Collects preoperative, operative, and postoperative data components for the program through the effective utilization of the hospital medical record systems
- Attends weekly Morbidity & Mortality conferences to ensure reliable data collection of postoperative occurrences
- Demonstrates applicability of the methodology and the reliability of definitions utilized by reviewers within the program through Inter‐Rater Reliability (IRR) testing
- Identifies streamlining and process improvement opportunities in the data collection process
- Demonstrates appropriate utilization of resources necessary to obtain valid, reliable data for entry into the Program
- Utilizes software applications for data collection and analysis
- Responsible for the accurate and timely entry of data into the program’s database and meets the caseload accrual requirement protocol
- Reviews weekly site accrual report on the database and responds to accrual report alerts
- Works Effectively with Patients, Families, and Staff
- Establishes effective working relationships with members of the hospital community, especially staff in the Surgery, Medicine, Nursing, Medical Records and the Information Systems Departments whose support is necessary for the management and success of the program
- Contacts patients and/or families via telephone and/or written communications postoperatively for the purpose of identifying possible occurrences associated with surgical procedures performed at the hospital
- Serves as an educational resource on the ACS NSQIP for internal and external audiences by developing educational material and delivering presentations
- ACS NSQIP Participation
- Successfully complete the ACS NSQIP SCR Training/Certification Program
- Participates in program teleconferences
- Attends national conference
- Minimum one year experience in hospital surgery department, surgery clinic, clinical research or medical records. Clinical chart review and abstraction experience required
- Ability to build relationships and gain alignment for clinical support and be able to articulate questions to receive an appropriate level of support from superiors and peers
- Ability to interact with all members of the surgical team and administrative staff in a professional and courteous manner
- Computer and Internet experience required ‐ familiarity and comfort with MS Office products is essential for success in this position (Word and Excel‐ required; PowerPoint and Access‐ preferred)
- Database data entry and/or management experience preferred
- Basic statistical knowledge preferred
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Research Nurse Resume Examples & Samples
- Excellent patient-care skills, excellent communication skills, to effectively communicate with patients and all members of the multi-disciplinary team
- Ability to take independent decisions, which have a moderate impact
- Ability to use initiative and creativity to resolve problems and identify and assess practical options
- Proficient in using common office IT packages (e.g. MS Office)
- A good understanding of confidentiality, data protection and safe record keeping and an understanding of ethical issues surrounding research involving patients
- RGN qualified or degree in Physiotherapy, clinical science or related subject
- Trained in and with experience in phlebotomy or willingness to be trained in the procedure
- Proven experience of working a multi-disciplinary team within a clinical setting
- Willingness to undertake further training within the field of musculoskeletal health
- Access to transport required for work at locations within South Wales
- Knowledge of clinical assessments (questionnaires, clinical scales, interviews) for movement disorders
- Proven experience of working with patients with musculoskeletal disorders either the hospital or community setting
- Knowledge of the research process
- Prior research experience
- Evidence of an interest in health research
- Nursing or other experience in health
- Flexible approach to work
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Research Nurse Resume Examples & Samples
- Relevant Degree/NVQ 4 or equivalent Professional membership/RGN Level 1 – current NMC registration
- Substantial experience of working as a research nurse
- Able to demonstrate professional knowledge within wound prevention and wound treatment to give advice and guidance to internal and external customers
- Ability to set up standard systems and procedures and make improvements as appropriate
- Evidence of ability to work unsupervised to deadlines, planning and setting priorities for own work and that of others and monitoring progress
- Postgraduate/Professional qualification
- Fluency in Welsh, written and oral
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Clinical Trial Research Nurse Resume Examples & Samples
- Cystic Fibrosis Knowledge
- Adept at electronic data capture (EDC)
- Critical thinking regarding disease management
- Pharmocology knowledge
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Research Nurse x Resume Examples & Samples
- Provide professional advice and guidance on the Genome Project, processes and procedures to internal and external customers, using judgement and creativity to suggest the most appropriate course of action where appropriate, and ensuring complex and conceptual issues are understood
- Investigate and analyse specific issues within the Genome Project, for example, patient recruitment issues, creating recommendation reports (including the supply of data as required to the Research coordinator(s)) supported by advances within the project
- Ensure that the provision of the project is delivered to the Institution, proactively changing the delivery according to customer requirements, specifically for this role to follow appropriate procedures to safeguard children, young people and vulnerable adults
- Collaborate with others in order to make recommendations for developments of established processes and procedures, in particular to liaise with other members of the 100,000 Genome Project team as needed to effectively run the Project and NHS Wales staff about operational aspects of the Project
- Establish working relationships with key contacts, developing appropriate communication links with the University’s Schools/Directorates and outside bodies as required
- Create specific working groups from colleagues across the University to achieve project and Divisional objectives
- To manage the Project on a day-today basis; co-ordinate case-load of participants for the project and supervise specific project teams on an occasional basis to accomplish key objectives
- Develop and deliver training as required within the team
- Undertake a variety of administrative duties to support the department
- Instruct and guide other employees across the University within Genome Project as required
- A degree in nursing (or a related subject) or relevant experience
- Current registration with the NMC or other appropriate governing body (e.g. HCPC)
- Substantial experience of working within a Research Nurse role
- Knowledge of research methods and techniques within specialist field
- Knowledge of genetics or genomics
- Knowledge of appropriate clinical research governance, systems and processes (with a particular focus on consent and mental capacity)
- Capability and drive to implement the study protocol
- Excellent organisational and team-working skills
- Evidence of collaborations with industry, NHS or social care
- Proven ability to work without close supervision and willingness to travel to research sites
- Proven ability to adapt to the changing requirements of the Higher Education community
- A willingness to take responsibility for academically related administration
- A commitment to high quality patient and public involvement
- Substantial experience of working within a research coordination role
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Research Nurse Resume Examples & Samples
- Participate in the recruitment and selection of participants for medical studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met
- Explain project to participant and enroll them into the study
- Schedule and/or perform medical testing such as drawing blood, taking blood pressure reading, testing for allergies and pulmonary function testing
- Maintain contact with participants throughout the project; search for participants that have changed addresses during the project
- Mail questionnaires to participants to complete or ask them questions by telephone or in person; compile results of questionnaires
- Perform procedures such as administering medications, measuring skin lesions, preparing patient for surgery and assisting physician in surgeries
- Provide medical information to the participants such as how to administer drugs and how to care for a particular illness
- Review medical records of study participants or possible participants to obtain relevant data
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Research Nurse Resume Examples & Samples
- Be current with appropriate emergency certifications and company emergency policy and procedures
- Utilize skills, knowledge, nursing diagnosis, and clinical judgment in order to provide a high standard of care for participants in clinical trials
- Utilize nursing assessment skills to observe participant general well-being and potential adverse events. Documents adverse events and takes appropriate action as needed
- Obtains Informed Consent and continues the ICF process by educating, explaining and informing participants of study procedures
- Administers investigational compounds (inclusive of parenteral) to participants according to the protocol and applicable regulations
- Performs study related activities such as IV insertion, telemetry, holters, vital signs, ECGs, venipuncture
- Collects and processes biological samples according to the protocol and Standard Operating Procedures
- Records data obtained according to the protocol and Standard Operating Procedures
- Ensures that client and participant confidentiality is maintained
- 0-1 related experience
- Additional experience may be substituted for education requirements
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Research Nurse Clinician Resume Examples & Samples
- Recruits, enrolls and follows subjects on infectious disease clinical trials
- Conducts the informed consent process with potential research subject in a sensitive and thorough manner
- Assures that studies are conducted according to
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Research Nurse NE Resume Examples & Samples
- Utilizes the nursing process as a basis for patient care
- Assesses research subject and completes nursing assessment, documenting findings in research subject records then, notifies physician of abnormal findings
- Establishes a care plan in collaboration with the research subject, family and research team to coordinate ongoing care
- Identifies discharge needs and facilitates discharge planning as appropriate
- Maintains professional relationships, including frequent and open effective communication with internal and external constituents
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Pediatric Research Nurse Resume Examples & Samples
- Assess, implement, and manage recruitment and study activities
- Interview and educate potential study volunteers and families
- Act as liaison between recruitment sites and study staff
- Conduct participant pre-screen calls and schedule participants for screening visit
- Conduct informed consent process
- Review medical records for basic inclusion/exclusion eligibility and assist in study enrollment
- Contribute in the development, implementation, and maintenance of standard operating procedures. Ensure studies comply with applicable regulations and guidelines, including Good Clinical Practice and Federal regulations. Implements and ensures compliance of QA/QC activities related to all studies
- Ensure security and confidentiality of all data
- Conduct chart reviews, preparation and maintenance of study materials, data collection including but not limited to study documentation, maintenance of volunteer’s medical and research records, maintenance of written study related logs and computer files
- Meet regularly (phone or in-person) with research coordinator for review of data accuracy and overall progress of recruitment activities
- Provide quality and compassionate nursing care, conduct research safety assessments, collect nasal rinse and blood specimens and communicate status of research activities to the study team. (The nursing activities may be performed in the CIR clinic, designated primary care provider offices, or in the volunteer’s home.)
- Engage in continuous professional development, training sessions and team meetings
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Research Nurse Resume Examples & Samples
- Ensure that the dignity, health, safety, and welfare of participants is given the highest priority at all times
- Respond to emergency situations based upon nursing standards
- Utilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials
- Obtains and documents medical history
- Handles participant complaints efficiently and effectively in order that their satisfaction is maintained
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Clinical Trial Research Nurse Resume Examples & Samples
- BA/BS degree in nursing or related health field preferred
- Responsible for the implementation of research vaccine protocol, documentation, data collection, and case management of study research subjects. Interview, prepare and educate patients, prepare and administer vaccine per MD order, develop long and short-term follow-up plans
- Complete study follow up according to protocol
- Assist regional research team as needed. Must be willing and able to travel to other sites as needed to support research team. Demonstrated ability to work independently and priorities
- Must be well organized, detail oriented and tenacious in follow through. Must posses the ability to work under pressure
- Must be able to make and complete accurate patient assessments. Demonstrate effective written, verbal and interpersonal communication skills. Possess proficient phlebotomy skills
- Minimum of 2 years experience as RN in Adult setting within the last 5 years preferred and some experience in pediatrics
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Research Nurse Resume Examples & Samples
- Assess patients as required by trial protocols. Will be required to take blood, test urine samples, performed spirometry and Feno assessment for which training has been given
- Responsible for the day to day running of designated observational research and take an active role in junior staff supervision, management and recruitment
- Assist in the informed consent process and provide ongoing information, education and support to Study patients and their caregivers
- Ensure study records are accurately maintained, including, but not limited to: records in nursing/medical notes, case report forms, trial site files. Ensure that hospital procedures and policies are followed
- Ensure Study protocols are followed and that studies are conducted in accordance with ethical principles that are consistent with the Declaration of Helsinki, International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) Good Clinical Practices (GCPs), Good Pharmacoepidemiology Practices (GPP) and applicable legislation for observational studies
- Lead on, and maintain an expert knowledge in sites portfolios open at the hospital / trust and for these portfolios: act as a reference point for team members, train team members, attend Multi-disciplinary meetings, and identify strategies for recruiting patients
- Provide, maintain and facilitate a high standard of clinical trial practice developing and promoting effective channels of communication both verbally and electronically. Network with multidisciplinary team to access expert knowledge and practice to facilitate trial patient journey
- Report site activity using study SRF
- Registered General Nurse or allied professional with at least 3 years post registration experience, including working in an acute setting, as you will be responsible blood tests ad sampling
- Ability to provide support to patients during their clinical trial experience
- Good knowledge of clinical trials, including, but not limited to: EU Clinical Trials Directive 2001/20EC, Good Clinical Practice for Clinical Trials and UK/Member State Statutory Instruments
- Well developed organisational skills and ability to multi-task
- Well developed interpersonal skills and ability to communicate effectively to a wide multidisciplinary team and patients
- Ability to work independently and be an excellent team player
- Competent in the use of computers at a basic level, including: Microsoft Word, Excel, Outlook, Access & Powerpoint and the Internet
- Flexibility to ensure achievement of objectives within constantly changing environments
- Experience in Asthma/COPD strongly desirable
- Experience in RAVE EDC System strongly desirable
- English language strongly desirable
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Research Nurse Manager Resume Examples & Samples
- Clinical knowledge and nursing skills as required by job responsibilities
- Communicate and work with a diverse team of professionals
- Function independently, multi-task oriented, and organized
- Healthcare setting
- Clinical Research
- Clinical Oncology
- Management/Leadership
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Research Nurse Coordinator Resume Examples & Samples
- Minimum of 1 year (or equivalent) of nursing experience
- Certification in Oncology Nursing preferred - OCN, AOCN, CPON, CCRP
- Demonstrated ability to work as an effective member of an interdisciplinary team
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Pediatric Research Nurse Resume Examples & Samples
- Screen, recruit and consent research subjects at both University of Colorado and Denver Health
- Accurate data collection and entry
- Collect and process research samples
- Manage patient tracking and follow-up visits
- Assist in the training and in-servicing of hospital staff on new study protocols
- Maintain research records
- Assist with monitoring study budgets and payment reconciliation
- Collaborate with other research personnel and groups on a variety of studies
- Maintain study specific certifications, human subjects protection training, computer training and other hospital required training
- A minimum of 2 years in an Obstetrical or Pediatric Setting
- Phlebotomy Skills
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Research Nurse, Nursing Resume Examples & Samples
- Assist with literature reviews and information analysis
- Participate as a member of the NEC-Zero research team to determine best NEC-Zero approaches
- Participate in collaborative research activities including data analyses related to NEC
- Assist in the designing of written information including documents and brochures related to NEC-Zero initiatives
- Perform NEC related duties including conducting literature searches for research
- May be assigned as mentor or supervisor for student interns/workers related to NEC-Zero initiatives
- Knowledge of the NEC-Zero Project and evidence supporting the treatment and care needs of necrotizing enterocolitis (NEC)
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Senior Research Nurse Resume Examples & Samples
- 50% - Primary role is to assist PI with supervision of staff in the implementation, management and coordination of research studies. 1) Writing and submitting IRB and GCRC applications, renewals, and amendments and assisting staff with necessary IRB training requirements, 2) Implements and maintains SOPs and will recommend changes to operational procedures as needed, 3) Based on study protocols will oversee the creation of study documentation and case report forms. Maintain MOP for each study assigned to, 4) Based on research protocols will oversee maintenance for the life cycle of the study, 5) Ensure that studies comply with applicable regulations and guidelines, including GCP, and that staff adhere to study protocols and procedures, 6) Ensure that study is conducted according to all applicable regulations and guidelines and adhere to standard operating procedures specified in protocol manual, 7) Act as contact between PI and other research sites and institutional partners, 8) Implement strategies for study recruitment and retention of participants. May act as primary contact for study participants, which may include scheduling, confirming appointments, and escorting/directing to various locations on/off campus, 9) Maintain working relationships with other study teams both internal to JHU and external to Pediatrics, 10) Ensure compliance of QA/QC activities related to all studies, 11) Schedule weekly progress meetings for active studies
- 15% - Data Management: 1) Oversee and/or perform the collection of study data, that includes ensuring data reflects the requirements of the study, 2) Abstract data from medical records or electronic files, 3) Oversee data entry into study database
- 20% - Nursing activities related to research include: 1) Patient assessment that may include, but is not limited to, skin testing, vital signs, nasal lavage/nasal blow techniques, saliva and blood specimens, 2) Participate in the open staff meetings to improve the research experience for our subjects, 3) Provide nursing care as needed for subjects/families in a research setting
- 15% - Supervision: Recruits, selects, develops, counsels, disciplines, and evaluates performance of employees to retain a diverse workforce; ensures compliance with human resources policies and procedures. Observes and assesses work; provides feedback; may provide technical supervision; develops knowledge, skills and abilities of staff, students, faculty and/or other clients; plans and supports employees in career development opportunities
- JHU Equivalency Formula: 18 graduate degree credits may substitute for one year of experience. Additional related experience may substitute for required education on the same basis. For jobs where equivalency is permitted, up to two years of non-related college course work may be applied towards the total minimum education/experience required for the respective job.*
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Research Nurse Coordinator Resume Examples & Samples
- Coordinates protocol implementation for clinical trials including but not limited to: preparation and submission of regulatory documents, patient screening and recruitment, informed consent, study enrollment, and participant follow up
- Communicates with sponsors, investigators, clinical monitors and colleagues to ensure effective clinical trial implementation and progress
- Initiates and maintains required clinical and regulatory files
- Participates in conferences, departmental meetings, continuing education, investigator meetings, site initiation, interim monitoring and close-out study visits as assigned
- Administers and/or dispenses investigation agents as needed
- Monitors patients' study progress to fulfill protocol and sponsor requirements
- Completes clinical course of study subjects as required per protocol, including, but not limited to, laboratory tests, vital sign measurement, EKGs, health status assessment and adverse event monitoring
- Prepares and analyzes regular reports of research activity, including MHRI monthly billing forms, IRB continuations & closures, and patient enrollment logs
- Assists MCRN staff and/or MHRI Investigators on study related activities, as required and/or as time allows
- Seeks opportunities to develop fund of knowledge in clinical study area
- Performs late stay requirements on a rotational basis, to ensure completion of study activities
- May be required to work off-hours & weekends for study-related activities
- Train new clinical research staff on the basics of clinical trials, basic clinical data analysis and serve as a resource when needed
- Assisting the supervision and assessment of Junior Research Staff during probationary evaluation
- Consistently demonstrates support for compliance in the performance of job duties and responsibilities by a) developing and maintaining knowledge of, and performing job functions in compliance with, rules, regulations, policies, and statutes that affect his/her job; b) maintaining knowledge of and performing job functions in compliance with MedStar Health and MedStar Health Research Institute policies and procedures; and c) reporting compliance concerns in an appropriate and timely manner
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Research Nurse Coordinator Resume Examples & Samples
- Screens and identifies potential research subjects according to established research protocol enrollment criteria
- Obtains informed consent from research subject or appropriate surrogate
- Ensures and monitors compliance with examinations, repeat examinations, treatments, and laboratory tests required by the protocol
- Identifies problems in the research design or analysis methodology and trends in patient reactions to treatment. Collects, organizes, catalogs, disseminates, and maintains appropriate files of current data
- Communicates with other hospital departments, staff and sites through in-services, presentations and collaboration to help with subject recruitment and participation
- Places IVs, draw blood and obtain other specimens as required
- May analyze and interpret data
- Attend periodic meeting off-site such as the NIH campus and surrounding metro DC hospitals
- Position may require periodic duties during evening or weekend
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Research Nurse Coordinator Resume Examples & Samples
- 1) Serve as a resource for oncology research protocols and related issues. Confer with sponsors, investigators, and staff regarding study issues
- 2) Maintain detailed knowledge of all components of oncology trial requirements and research procedures, ensuring protocol adherence. Communicate specialized knowledge of research studies, research methodologies and practices to all appropriate persons
- 3) Maintain awareness, and possess working knowledge, of applicable federal, state, local, and other regulations and guidelines pertaining to departmental research. Implement and apply these regulations in the conduct of research work to ensure the highest quality research activities from site selection through study closure
- 4) Identify and screen potential study participants. Discuss protocol participation with potential participants and others as indicated. Verify participant eligibility according to protocol specific criteria
- 5) Coordinate and finalize the informed consent process for study participants according the departmental, institutional, state and federal regulations and guidelines. Document informed consent process
- 6) Effectively facilitate participant accrual to appropriate trials, while ensuring adherence to human subject protection and other research guidelines. Collaborate with Investigator, and sponsor as applicable, to determine appropriate eligibility maintaining all required documentation for eligibility verification
- 7) Manage multiple trials and work with appropriate support staff/departments to ensure study requirements are met. Ensure completion of all tests/procedures/assessments within indicated protocol/project timeframes. Provide clear and appropriate documentation for all study related activities
- 8) Design tools and maintain materials that aid in the accurate data collection, reporting and conduct of the study and in compliance with Good Clinical Practice. Recommend changes/additions to established data forms where appropriate. Utilize resources to enhance efficient patient accrual, protocol implementation, protocol maintenance, working together with investigators and other research colleagues throughout the protocol life cycle
- 9) Monitor the course of study participants, reporting all required side effects, deviations, disease status, and other data related to protocol adherence in an accurate manner within protocol, sponsor and IRB timeframes. Complete and maintain required records of study activity including, but not limited to: case report forms, research files, adverse event reporting, database records, and thorough source documentation substantiating all reported data
- 10) Demonstrate good judgment to make decisions, adjust priorities, and manage schedule to ensure that accurate work is accomplished within the required timepoints. Utilize critical thinking to collect, analyze and evaluate all relevant information prior to taking action
- 11) Adhere to protocol specific and local requirements while accurately and completely coding and submitting data and materials in a timely manner. Ensure data quality and integrity in research databases for each stage of data collection. Assist in collection, preparation, and analysis of information for institutional special reviews and/or studies; Collaborate with investigators and research team in development of special projects or initiatives
- 12) Prepare regular reports of research activity including, but not limited to: assisting in preparation of data safety monitoring reports, protocol-specific patient reports/chart review, and pre-inspection reports.Consistently ensure regulatory readiness for external inspection and sponsor monitoring visits. Respond to follow-up requests as needed
- 13) Attend conferences, training programs, departmental research meetings, sponsor-initiated meetings, workshops, seminars, webinars as assigned, to keep abreast with project objectives, acquire new and/or updated knowledge in area of expertise relevant to current position. Prepare for, and facilitate, meetings as appropriate. Share information gained with pertinent staff
- 14) Function as a liaison between the Washington Cancer Institute (WCI) research program and those within the MedStar Georgetown Oncology Network in relation to clinical research and protocol-specific conduct. Facilitate discussions, and meetings, as required with Network Investigators, research staff and WCI protocol research team. Participate in protocol-specific start-up and progress meetings in support of Network objectives as needed
- 15) Integrally involved in facilitating research billing processes including, but not limited to: being the 'gate-keeper' in steering all research-related services to the appropriate billing category –Help in the patient-care costs (both billable and non-billable) process to ensure that research non-billable services (where research is guarantor) are not billed to study participants or insurers
- 16) Work together with the Business/Administrative division of the department in facilitating the Medicare Coverage Analysis process. Ensure Medicare clinical trial billing forms are submitted to providers as applicable. Assist in billing reconciliation process as needed. Abide by MHRI policies regarding Medicare billing, attending any billing training modules as directed. Participate in and promote the prevention, detection, and resolution of instances of noncompliance with departmental and institutional billing policies and procedures
- 17) Consistently demonstrate support for compliance in the performance of job duties and responsibilities by a) developing and maintaining knowledge of, and performing job functions in compliance with, rules, regulations, policies, and statutes that affect his/her job; b) maintaining knowledge of and performing job functions in compliance with MedStar Health and MedStar Health Research Institute policies and procedures; and c) reporting compliance concerns in an appropriate and timely manner
- 18) Provide education and counseling to research patients and families related to pertinent aspects of their protocol(s), as well as health care staff and referral resources as applicable
- 19) Take part in discussion concerning toxicity determination, side effects, adverse events and other safety considerations for study participants
- 20) Support the research process by taking part in clinical interactions for research purposes including, but not limited to, administering injectable study medications, performing phlebotomy in specific research scenarios (i.e., pharmacokinetic draw schedules), performing study-directed ECG testing, and entering treatment orders to the patient's medical record according to protocol requirements
- 21) Perform other duties as assigned
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Research Nurse Coordinator Resume Examples & Samples
- Conduct and document all clinical and clinical research activities in accordance with standards of good clinical practice, JCAHO guidelines, research protocols, and hospital policies and procedures
- Assess patients' physiologic condition upon admission/intake, throughout inpatient stay or outpatient visit, and upon discharge/exit; planning, implementing, evaluating and documenting care provided, per protocol requirements and standards of good clinical practice
- Administer drugs via route ordered, documenting in medical records and on case report forms in appropriate places
- Observe patient reactions to drugs by using subject behavior, known facts about drugs in study, and document on case report forms all requested information by protocol. Report adverse drug reactions to the WHC Principal Investigator and in accordance with the protocol for reporting adverse events, and in accordance with IRB and hospital policy
- Start and maintain intravenous (IV) lines, draw blood as necessary for clinical and research needs. Dispose of used materials in accordance with OSHA, JCAHO, and hospital procedures
- Collaborate with MGTI Investigators and Physicians, Georgetown CRCs or staff, transplant coordinators, Clinical Nursing Managers, Staff Nurses and others necessary in implementing protocols on units and outpatient settings
- Act as a member of the research team, delivering direct patient care, and reporting and documenting observations orally and in writing as necessary to GUMC/MWHC Principal Investigators, Patient Care Managers, or Clinical Supervisor
- With appropriate training and certification in human research protection issues, obtain informed consent after confirming eligibility
- Keep Study Coordinator/Clinical Supervisor informed of the progress of protocols and any problems with recruitment, retention, or study implementation
- Enter clinical and research data into case report forms, or computer systems using established software, as needed. Create source documentation that is clear and follows guidelines put forth by protocol team ensuring data quality and compliance with IRB for confidentiality/HIPPA protection. Maintains organizational systems needed for patient visits, calendars, and follow-up on study visits. Establishes systems as needed to facilitate patient enrollment and retention. Assist and manage monitoring visits and internal audits to track study progress and improve data quality
- Attend weekly meetings as needed with other members of the research team for applicable protocols. Travel to Georgetown as needed for meetings
- Develop teaching materials for nursing in-services
- Availability for on-call nights/ weekends
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Senior Research Nurse Resume Examples & Samples
- Protocol Management Assumes responsibility for the effective operation of research protocols in collaboration with the principal investigator and study sponsor. Examples include participation in SIVs, conference calls, interim assessments and email/written business correspondence. If required by the protocol, ensures capture of research-associated tests and procedure charges to the research financial account. Assesses patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient settings. On a real-time basis, assesses the patient’s clinical status; coordinates, evaluates and follows the patient’s participation in clinical trials. Collaborates with the entire medical care team as necessary. Provides documentation in the patient’s medical record, protocol specific documents, and institutional requirements. Communicates availability of protocol treatments for accrual. Participates in the development and maintenance of the protocol-specific order sets. Maintains the institutional patient regulatory protocol requirements (deviation logs, SAEs, AE logs, IRB continuing review, etc.) Notifies clinical and/or research laboratories of protocol-required laboratory tests including EKGs, PKs, PDs, urine collection, etc. Prepare orders for protocol-related tests, procedures, consults, requests for pathology slides and blocks as needed
- Protocol Data
- Patient Education and Professional Education
- Assist in identifying deficient areas of the program and communicate these deficiencies along with potential resolutions to the Research Nurse Manager(s). Positively approach difficult and/or negative situations and seek resolution. Identify, communicate, and aid in SOP development and establishment of guidelines and processes in an effort to improve efficiency and overall conduct of the research program
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Research Nurse Resume Examples & Samples
- Assumes responsibility for the effective operation of research protocols in collaboration with the principal investigator and study sponsor. Assesses patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient settings. Coordinates, evaluates and follows the patient’s participation in clinical trials. Collaborates with the multidisciplinary team as necessary. Provides documentation in the patient’s medical record or recruitment log per protocol and institutional requirements. Identifies and develops methods of patient recruitment. Assists with protocol development including budget issues and protocol design. Acts as a liaison with sponsor institutions and pharmaceutical companies conducting research studies
- Assists the primary investigator in collection and evaluation of data. Evaluates response to treatment, treatment toxicities and adverse drug reactions and reports appropriately to the principal investigator, the Institutional Review Board and the study sponsor. Provides protocol summary reports as requested. Assists with protocol analysis. Utilizes computer statistical/data management packages as necessary. Designs research tools to aid in data collection and analysis
- Participates in protocol-specific clinical tasks as needed. Identifies and provides patient and family educational needs regarding treatment management, evaluation and follow-up in clinical trails through talking with patients person-to-person or by telephone and/or through written educational material. If necessary, administers investigational medications, following acceptable nursing procedures/guidelines. Collects and properly identifies special lab specimens as required by protocol by drawing blood and collecting specimens provided by patients, following accepted nursing and laboratory procedures/guidelines. Orders protocol - related tests, procedures and consults and obtains pathology slides and blocks as needed
- Provides professional and ancillary staff education concerning research protocols by presenting in- services in clinic and inpatient units and by provided clearly understood written and/or computerized directions to the hospital and/or clinic staffs as each new protocol is introduced. Provides accurate information as requested to the multidisciplinary team, consumers and professional public organizations. Keep current concerning oncology and data management issues through reading and/or attending meetings/inservices. Presents data from clinical trials in publication and or formal oral presentations
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Research Nurse Resume Examples & Samples
- Assessment: Screens patients for protocol eligibility and participation in clinical trials that may require the analysis of patient data and charts using visual acuity to determine eligibility. These duties may require frequent bending and stooping to access patient data and charts that may weigh up to ten pounds. Specific duties may include
- Assessing in-patients and/or out-patients for protocol eligibility
- Identifying patient and family education needs regarding treatment and follow-up on specific clinical trials
- Identifying nursing staff in-service needs regarding administration and monitoring of patients on specific clinical trials
- Administer protocol survey to patients
- Intervention: Participates in the coordination and monitoring of patient treatment in clinical trials. Specific duties may include
- Scheduling tests before, during, and after treatment
- Administering investigational and non-investigational medications as required by the protocol
- Obtaining pharmacology and other required laboratory specimens for research purposes
- Monitoring patient responses during treatment on clinical trial and performing general follow-up as required by protocol
- Teaching patient and family about administration and side effects of medication
- In-servicing nursing and technical staff on the management of patients in specific clinical trials
- Executing primary research design including double and single blind studies
- Collects blood samples for the protocol project. This will require veni-puncture skills with a steady hand and arm posture and follow accepted institutional procedures for collection of specimens
- Maintain records in endoscopy database as required by primary investigator
- Evaluation: monitors, and in collaboration with the physician, evaluates patient response to
61
Research Nurse Resume Examples & Samples
- Coordinate activities related to initiation and conduct of clinical trials
- Work with staff in Patient Business Services to develop research charge tickets for protocols
- Interact with clinic staff to make sure research charge tickets are used appropriately and that billing to sponsored study accounts is accurate
- Timely notification of patient on study to patient access coordinator and PBS
- Screen patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient settings
- Instruct co-workers in allied fields in procedures for recording patient information
- Maintain data necessary for audits
- Understand and adhere to the policies and procedures related to conduct of clinical trials as delineated in the department training manual and presented at weekly training meetings
62
Clinic Research Nurse Director Resume Examples & Samples
- Demonstrated computer skills, and proficiency with MS Office Suite programs
- Demonstrated knowledge of GCP and ICH and the application to the conduct of clinical trials
- Thorough understanding of cross functional clinical processes including clinical supply and data management
- Strong analytical and problem solving skills, with the ability to generate successful approaches to addressing issues that arise in the implementation of each study
- Demonstrated organization and prioritization skills, and ability to handle multiple tasks with competing deadlines
- Exceptional interpersonal and collaborative skills, with the ability to interact effectively with a diverse constituent population in a constructive and engaging manner
- Excellent written and verbal communication skills
- Demonstrated supervisory skills
- Strong attention to detail
63
Research Nurse Resume Examples & Samples
- Responsible for the day to day activities involved with research protocols including pre-screening, scheduling, consenting, data collection, data entry, and query resolution
- Responsible to achieve set goals in demographic and numeric recruitment of qualified English and Spanish speaking subjects in a variety of age groups
- Provide direct patient care involving lab draws (in infants, children, and adults), administering medication, and performing tests such as electrocardiograms and allergy tests where an RN license is required
- Assess participants during clinic visits and over the phone to determine if patients are experiencing side effects or other problems, and notifies principal investigator if problems arise
- Responsible for providing medical information to the participants such as how to administer drugs and how to care for a particular illness
- Schedule and/or coordinate the scheduling of required laboratory tests, imaging, or exams
- Perform study related procedures including the administration of questionnaires and conducting pulmonary function testing including spirometry, IOS, ENO, sputum induction and other pulmonary function testing of both child and adult participants enrolled in our clinical research studies
- Provide periodic training to other research staff members to assure understanding of emergency protocols and patient safety
- Direct experience in human subject’s research
- Experience in respiratory related research
64
Research Nurse Resume Examples & Samples
- Protocol Management: Applies clinical and research knowledge of protocol conduct in the effective management of research protocols. Participates in fiscal activities related to clinical research. Communicates effectively with research team. Documents and organizes protocol related items consistent with protocol guidelines, institutional and departmental policies, GCP and Federal Regulations
- Data Management: Demonstrates knowledge of research process, Code of Federal Regulations and ICH Guidelines for Good Clinical Practice (ICH-GCP). Demonstrates competence in key aspects of data collection and data entry incorporating institutional guidelines. Demonstrates knowledge of the current NCI-Common Toxicity Criteria and institutional reporting requirements. Knows how to ensure the quality of protocol specific data
- Clinical Practice: Applies the nursing process and incorporates national and institutional standards of nursing practice in delivering nursing care to patients enrolled in research protocols. Demonstrates clinical competence in aspects of care incorporating institutional guidelines and protocol policies. Documents patient care and outcomes per institutional, federal and protocol standards
- Education/Team Orientation: Applies principle of teaching/learning process to patient/family learning needs. Identifies experiences to increase knowledge and participates in educational activities
- Communication/Respect: Uses appropriate communication skills with patients. Accepts and incorporates constructive feedback into professional practice. Can locate and utilize institutional and departmental policies and procedures
65
Research Nurse Coordinator Resume Examples & Samples
- Applicants without a BSN degree must actively pursue and attain a BSN within 6 years of hire
- Continued employment by Swedish beyond 6 years is contingent upon attaining the BSN degree
- Current Washington State RN License
- Minimum 2 years experience within specified research field
- Working knowledge of Microsoft Office software
- Oncology or Chemotherapy certification highly preferred
- Previous experience in any of the following disciplines: Hematology/GI/GU/GYN/Lung/Breast
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Research Nurse, Senior Resume Examples & Samples
- Participate in protocol review to evaluate feasibility
- Supervise research nurses and study coordinators when assigned
- Coordinate and/or perform physical assessments required by research protocol such as blood pressure readings
- Recruit study participants by referrals or by placing advertisements on television, radio or in newspapers; schedule appointments, interview and evaluate potential participants to ensure they meet eligibility requirements; instruct participants concerning protocol and obtain consent signature
- Provide direct patient care involving diagnosis, administrating medication and performing tests such as glucose tolerance test, infusions and electrocardiograms
- Observe and monitor the physical and mental status of study participants throughout the study visit
- Assess participants for evidence of drug toxicity, unexpected side effects or other problems and notify principal investigator
- Communicate in a timely manner to study team of all notable participant issues
- Assure proper documentation is in each study participant’s record
- Handle telephone inquiries in a professional and courteous manner
- Utilize universal precautions in any potential contact with study participant’s bodily fluids or used participant supplies that may be contaminated with participant’s bodily fluids
- Additional duties may be assigned as it relates to this position
- Knowledge of basic computer skills
- Ability to interpret, adapt, and apply guidelines and procedures
- Ability to communicate clearly, both oral and written
- Meticulous attention to detail
- Skill in organization and record maintenance
- Ability to complete paperwork with precision
- Ability to work independently as well as in a team environment
- Experience in Human Subjects Research
- Fluent in speaking, reading & writing Spanish
- Experience with regulatory work related to human research clinical trials
- Understand research terminology, biology, and knowledge of Good Clinical Practices as demonstrated by prior job experience
- Demonstrate ability to maintain multiple research trials and large study population demands effectively and independently of others
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Research Nurse x Resume Examples & Samples
- Take responsibility for resolving issues independently within the project deliverables where they fall within set role objectives
- To work in accordance with NMC code of professional conduct and relevant professional, government and Trust policies for the delivery of patient care in the clinical trials / research setting
- Job description continued in Additional Information section**
- RGN Level 1 with current NMC registration
- Knowledge of research methods and techniques in non CTIMP clinical research studies
- Able to demonstrate professional knowledge within genetics or genomics to give advice and guidance to internal and external customers
- Evidence of ability to solve expansive problems using initiative and creativity; identify and propose both practical and innovative solutions
68
Research Nurse Resume Examples & Samples
- Provides patient care utilizing the nursing process with an interdisciplinary approach, following established nursing procedures and standards
- Provides education to the patient and significant others
- Identifies measures to enhance the physical, psycho-social, and spiritual well being and increased comfort
- Demonstrates accurate documentation in the patient's medical record
- Serves as a resource for ancillary staff regarding management of patient care
- Displays professionalism and teamwork. Demonstrates leadership and accountability for the efficient operations of the office
- Interfaces between clinical staff, the Office of Sponsored Research, Research Administration, PIs, clinical research staff, and external entities to identify clinical research pipeline and completes protocol budgeting, feasibility, and initiation
- Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study
- Completes required follow-up and active patient monitoring per study protocol at one or multiple sites of service
- Plans, coordinates, and manages all activities pertinent to the specific clinical trials, ensuring patient safety, good clinical practices, and compliance with the protocol and regulatory agencies
- Completion of an accredited Registered Nursing program required
- Current PA RN License required
- Minimum 1 year nursing experience and experience in venipuncture and with venous access devices required
- BSN Degree in Nursing and completion of a Comprehensive Cancer Chemotherapy course preferred
69
Mental Health Research Nurse Resume Examples & Samples
- Evaluate the appropriateness of a subject for participation in brain imaging research; conduct a clinical assessment concerning the degree to which a child, adolescent, or adult meets safety criteria for entering a magnetic resonance imaging (MRI) environment
- Work with children, adolescents, and adults receiving an MRI exam; assist MRI technologists as they prepare patients for a brain imaging examination; alert the MRI technologist to safety concerns during this process; attach physiology monitoring equipment to a patient in an MRI environment
- Evaluate the degree to which a child, adolescent, or adult exhibits clinical distress in the context of an MRI examination; work with the research participant and family to reduce stress that arises in the context of an MRI examination and work with other staff to determine when the level of stress appears of sufficient severity that MRI examination should cease
- Address any concerns that arise from families and research participants following completion of an MRI examination
- Screen patients for the projects, which focus on children with anxiety disorders, a behavioral inhibited temperament, major depressive disorder, bipolar disorder or extremely severe, impairing irritability and their families; conduct structured and semi-structured interviews with probands, and parents and siblings of probands; provide clinical support to patients and families throughout the time that they are participating in research protocols
- Provide family support and crisis management services as needed
- Provide referral to appropriate NIH resources and community services, when indicated
- Participate in the planning and execution of clinical research in the capacity of clinical support staff
- Conduct screening/baseline evaluations in collaboration with staff
- Administer and score a wide range of complex structured and semi-structured interviews (such as the SCID, the K-SADS and many others) to the child and adolescent probands and the parents of the probands
- Conduct accurate preliminary evaluation of potential probands through extensive telephone interviewing of parent, review of medical records, consultation with treating professionals, and consultation with NIMH medical staff, leading to acceptance for on-site evaluation or rejection with referral if indicated
- Conduct frequent assessments to monitor the participants’ progress and the effectiveness of therapeutic protocols
- Participate in research group meetings and in the decision making process regarding patient inclusion in the studies, patient and parent diagnosis, and patient and family management throughout participation in the research protocol
- Make recommendations for appropriate referrals, including Child Protective Services, psychotherapy, community services involvement, special education, or activity programs
- Locate, evaluate and maintain contact with community organizations and facilities such as day treatment centers, clinics, etc
- Document research and clinical findings
- Participate in collection, storage, and analysis of data regarding neuropsychological function and the life course of illness in patients as ascertained by testing and interviews with proband and family members
70
Oncology Research Nurse Resume Examples & Samples
- Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol
- Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability
- In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug, and thoroughly documents all findings
- Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities
- Maintains regulatory documents in accordance with USOR SOP and applicable regulations
- Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research
- May collaborate with Research Site Leader in the study selection process
- Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors
- Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality
- May be responsible for compiling and reporting protocol activity, accrual data, and research financial information to practice administration and physicians
- May oversee the preparation of orders by physicians to assure that protocol compliance is maintained. Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting
- Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law
- Graduate from an accredited program for nursing education (BSN preferred)
- Minimum of 2 years of Oncology RN experience required
- Experience in clinical research preferred
- Current licensure as a registered nurse in state of practice
- OCN, SoCRA or ACRP certification preferred
- Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials and GCP concept
- Attention to details and accuracy
- Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents
- Ability to work independently, organize, prioritize, and follow through with results
- Ability to solve practical problems and implement solutions
71
Research Nurse Resume Examples & Samples
- Coordinates the implementation and conduct of research projects to ensure adherence to research protocol requirements such as; timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of serious adverse events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines
- Assesses research subject; completes nursing assessment, documenting findings in research subject records. Notifies physician of abnormal findings
- Establishes a care plan in collaboration with the research subject, family and research team
- Coordinates ongoing care. Identifies discharge needs and facilitates discharge planning as appropriate
- Directs, coordinates and participates in the evaluation and supervision of nursing care provided to research subjects to establish patient care priorities and delegate nursing activities according to the patient needs and staff qualifications and capabilities
- Provides and documents education
- . Conducts and documents the informed consent process
72
Research Nurse Resume Examples & Samples
- Specialty/Department/Practice –Oncology Research
- Shift/Schedule – Day Shift
- Associate’s Degree Required
- 1 Year Experience Required
73
Research Nurse Coordinator Resume Examples & Samples
- Collaborates with other nurses in the health system and with outside collaborating centers. Shares research education with other nurse and disciplines. Has demonstrated management of a clinical research protocol independently
- Assess subject and family educational needs about the informed consent process, protocol intervention procedures, and its relationship to the disease process
- Performs accurate and safe procedures within the scope of practice of research nursing: (specimen collection, serial blood drawing, venous and central access with the exception of A lines. Stimulation testing, administration of blood products, fluid and research documentation
- Administering and overseeing injections of contrast medium and radio-tracers (solutions that enable the area of the body being imaged to show more clearly on the images or pictures)
- Administer stock medication safely and with knowledge of hospital policy and procedure. Administer selective research medication safely with accountability and knowledge of its effect within the protocol domain and CRC guidelines
- Sets priorities based on subject care and protocol requirements. Communicates through verbal, written, and computer methods effectively with all members of the health care team. Works with staff in a team approach to assist subject/protocol needs and will extend beyond the completed assignment to assist others
- Reviews each protocol prior to subject entry and addresses questions or concerns to the appropriate personal (Operations Manager, Principal Investigator, imaging technologists). Create protocol flow sheet to identify a brief summary of the protocol requirements for all staff nurses. Develop, implement, and evaluate a plan of care for each subject incorporating short and long term goals and expected outcomes of each
- Demonstrates appropriate clinical skills relating to the execution of research protocols. Demonstrates the ability to assess situations and make critical decisions affecting research procedures
- Effective documentation, observing any changes in a subject’s status and response to the protocol. Maintain effective communication at all times. Educate research subjects and families about the clinical study and maintain optimal health. Participates actively in the informed consent process
- Demonstrates critical nursing judgment to maintain the integrity of the research protocol without compromising subject safety
- Demonstrates the ability to practice independently within study guidelines
- Provides direct care to the research subjects utilizing the nursing process with knowledge and understanding of the purpose and methodology of the protocol
74
Research Nurse Coordinator Resume Examples & Samples
- Collaborates with other research coordinators and nurses in the health system and with outside collaborating centers. Has demonstrated management of a clinical research protocol independently
- Performs accurate and safe procedures within the scope of practice of research nursing: (specimen collection, serial blood drawing, venous and central access
- Administering and overseeing injections of contrast medium and radio-tracers
- Administer stock medication safely and with knowledge of hospital policy and procedure
- Demonstrates appropriate clinical skills relating to the execution of research protocols
- Demonstrates the ability to assess situations and make critical decisions affecting research procedures
- Demonstrates critical nursing judgment to maintain the integrity of the research protocol without compromising subject safety. Demonstrate the ability to practice independently within study guidelines
75
Research Nurse Resume Examples & Samples
- Participates in discussions regarding feasibility of protocol implementation based on knowledge of institutional capabilities and limitations, therapy, or population of interest
- Ensures initial and ongoing consent process is performed and documented in compliance with the U.S. Food and Drug Admin¬istration (FDA), Good Clinical Practice, institutional policies, sponsor requirements, Institutional Review Board (IRB) and other applicable regulations, guidelines and policies
- Participates in the education of research subjects, families and health team members regarding study and significant new information arising during the conduct of the trial
- Collaborates with Principal Investigator (PI) to ascertain study patient eligibility for a clinical trial, including documenta¬tion of criteria specified in the protocol. Identifies and develops processes to overcome recruitment barriers
- Adheres to the protocol and other applicable requirements. Performs required procedures such as include administration of investigational agent (under PI supervision), electrocardiograms, placement of IV, catheters, phlebotomy, specimen collection, vital signs, subject assessment/questionnaire completion, adverse event assessment
- Collaborates with PI to assess patients for adverse events; documents and reports findings per protocol, FDA, sponsor, and IRB policies. Evaluates disease response results and physical assessment data in conjunction with the PI to determine response per the protocol (as applicable). Discusses protocol changes with PI, as necessary
- Administers, scores and evaluates assessments as assigned and as related to the study protocol. Collects data, confers with PI and forwards results to internal and/or external sponsors
- Collaborates with physicians, investigators, and other healthcare providers regarding subject care and safety as necessary. Promotes respect and advocates for the safety and care of clinical research subjects
- Facilitates and participates in the preparation for and implementation of audits including but not limited to the FDA, IRB and other external and internal monitors and auditors
- Interfaces with the Office of Grants and Contracts (OGC) and IRB to ensure all documents are processed and maintained per applicable regula-tions
- Collaborates with PI to organize all phases of grant process for submission to funding agencies and adherence to clinical trial agreement/study budgets, as required
- Ensures investigational agent availability and accountability
- Bachelor’s Degree in Nursing, required
- BCLS, ACLS, preferred
- Minimum of three (3) years nursing experience required, including one (1) year experience in Clinical Research, preferred
76
Research Nurse, Stem Cell & Gene Therapy Resume Examples & Samples
- Demonstrated ability to work with research subjects of all ages and backgrounds
- Verbal and written communication skills to convey medical and research-related information to research subjects of all ages and backgrounds
- Ability to identify confidential and sensitive information (written and verbal)
- Ability to implement good clinical practices in all interactions with study participants, their families, and colleagues
- Ability to provide work direction to research support staff
77
Senior Research Nurse, Outpatient Resume Examples & Samples
- 5 years of clinical or related experience
- 3 years of experience in clinical research with knowledge about the conduct of clinical trials, research principles, and methodologies/study design
- 3 years of pediatric clinical experience
- Master of Science degree
- Pediatric Advanced Life Support (PALS) certification
- Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA) Certified Research Associate (CRA), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or comparable
- Clinical or related experience in the subspecialty of involvement
- Working knowledge of basic statistics
- Broad knowledge of federal regulations and regulatory requirements for conducting research with the ability to mentor
- Good computer skills, including working knowledge of a PC and Microsoft Office (Word, Access, Excel, and PowerPoint)
- Must be able to successfully pass the Basic Windows Skill Assessment at 80% or higher rating within 30 days of employment
- Self-directed and motivated to work independently toward short- and long-term goals
- Must possess good communication, organization, and interpersonal skills
- Develops, conducts, and facilitates research protocols at an expert level
- Provides substantial support for investigators in writing study protocols
- Leads participant screening, enrollment, study activities, and communication
- Coordinates study visits and procedures, including specimen acquisition, transport, documentation, shipment, and monitoring process for services
- Acquires equipment and supplies resources for research studies
- Obtains informed consent by following Children’s Healthcare of Atlanta policies, procedures, and regulatory requirements
- Schedules study-specific visits in conjunction with ancillary departments
- Oversees and provides direct patient care to conduct research protocols
- Provides orientation and mentoring to nursing staff regarding direct nursing care according to Children’s Healthcare of Atlanta standards of practice
- Completes phlebotomy for the acquisition of research specimens
- Administers research medications under a study-specific protocol
- Completes nursing physical assessment, vital signs, and venous access
- Completes clinical assessment and safety evaluation of study subjects and notifies Principle Investigator when appropriate
- Reviews and grades adverse events, concomitant medications, vital signs, and lab results and notifies Principle Investigator when appropriate
- Provides health education to participants as part of a study protocol
- Monitors nursing documentation and order entry within the medical record
- Facilitates all regulatory processes related to clinical research activities at an expert level
- Prepares, submits, and modifies Institutional Review Board reports and handles reporting and termination activities
- Structures the maintenance of all regulatory documents
- Leads others in sponsor correspondence, monitoring, and study meetings
- Guides interdepartmental auditing of regulatory practices
- Facilitates data management activities at an expert level
- Develops and evaluates source and case report form tools
- Manages data entry and ensures data integrity
- Supports statistical services needs
- Collaborates with manager to assess data management needs
- Participates in and acts as a mentor for quality and education activities
- Monitors compliance throughout all study activities
- Engages compliance oversight as needed
- Leads education activities and quality initiatives to support specific research activities and primary role at Children’s Healthcare of Atlanta
- Maintains all licensure, certification, and system education requirements for role
- Coordinates educational activities related to study needs for study staff, investigator team, and patient care staff
- Initiates departmental policy and quality projects
- Collaborates with manager to incorporate system initiatives into departmental practices
- Serves as a resource facilitating grants, contracts, and financial tasks for research and clinical trials
- Independently provides services for investigators in study budgeting, sponsor interactions, routing, feasibility assessments, account management, and reconciliation
- Serves as a collaborator and key contact for key business partners, including Emory, Georgia Tech, and University of Georgia
- Works collaboratively with manager to monitor metrics
78
Research Nurse Resume Examples & Samples
- Follows all protocol related requirements. Demonstrates the knowledge, skills and ability to perform required research nursing duties on phase I, II, and III clinical trials
- Provides consultation, support and education to patients and families as needed
- Provides leadership to clinical research coordinators and other ancillary staff regarding assigned protocols and trial-related requirements
- Practices safe environmental and/or infection control methods
- Advises supervisor, physicians, nurses and sponsors of potential or actual problems
- Participates in planning, workshops, evaluation meetings, seminars, educational and/or administrative meetings as necessary or requested
- Reviews and adheres to departmental policies and procedures to maintain proficiency in operating guidelines
- Provides accurate and complete source documentation for patients participating in research protocols. Documents concomitant medications and adverse events accurately per FDA and GCP guidelines
- Validates patient/family understanding of study requirements, risks and benefits by assisting the physicians in obtaining informed study consent
- Accurately calculates study medication dosages, completes appropriate orders, and follows all standard operation procedures
- Performs clinic assessments for assigned patients and accompanies MD on patient clinic visits
- Works closely with clinical research coordinators and data managers to complete case report forms and meet all data entry guidelines
- Assists research staff in responding to data queries
- Follows all FDA, GCP and ICH guidelines for study conduct in the care of patients on research protocols
- Seeks guidance and direction, as necessary, for the successful completion of job duties. Asks appropriate questions when in doubt
- Communicates well with research nursing team and with management. Keeps supervisors/management apprised of important departmental concerns and issues
79
Research Nurse Coord Resume Examples & Samples
- Provides educational services to research participants and family regarding study participation, participants current clinical condition, and or disease process
- Assesses/documents adverse events as reported by research participants, works closely with PI to document according to department process (grade, attribution, treatment, etc), reports to regulatory and sponsor as required
- Records research data where assessed or reported by patient (ie. symptoms of treatment)
- Participates in the query and analysis of research data
- Facilitates the education of the interdisciplinary team on study requirements
- Collaborates with the interdisciplinary team to create and communicate a plan of care that allows for safe and effective collection of clinical research data
- Coordinates research participant study visits
- Triages patient by phone and provides clinical information to the patient
- Recruits of study participants and/or oversees the recruitment of study patients
- Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities and/or has oversight of the research activity
- Coordinates study participant interventions as required and/or has oversight of the research activity
- Serves as a liaison between study participant and PI, Clinical Research Nurse and other research staff
- Prepares data spreadsheets for Investigator and/or department
- Prepares and updates investigation binder
- Completes Case Report Forms
- May prepare IRB submissions
- Assists with data compilation
- May assist with grant proposals, publication preparation, and presentations
- May coordinate grant activities post award through closure (monitoring budgets, compliance, progress reports)
- Assists with the education of junior-level staff
- Has general oversight of research portfolio as it pertains to the clinical coordination of the studies
- May process, ship, track or otherwise handle research specimens
80
Research Nurse Resume Examples & Samples
- Perform data management of an administrative and scientific nature using the Cardiac Surgery clinical quality and research database. Provide a range of support to include data compilation, documentation and entry into the database of all eligible patient cases for the purposes of quality data reporting to regulatory and other agencies. Ensure the accuracy of data for reporting to state regulatory agency
- Ensure data is entered in a timely and accurate fashion. Collect, analyze and assure the quality of patient documentations as well as maintain confidential patient files
- Provide reliable collection of preoperative, operative, and postoperative components for heart cases
- Collect reliable, valid data for comparative risk-adjusted outcomes of Cardiac Surgery
- Appropriately utilize resources necessary to obtain valid, reliable clinical data
- Utilize clinical knowledge to analyze data and identify trends and patterns
- Attend monthly Morbidity & Mortality meetings to collect incidences of negative postoperative occurrences
- Select and utilize applicable methodology and reliability of definitions and reviewers through inter-reliability testing
- Identify and address areas for streamlining and process improvement in the data collection process
- Elicit support necessary to obtain valid, reliable data for reporting to regulatory agencies
- Maintain up-to-date knowledge of regulatory changes of definitions and variables for reporting data
- Train new fellows and attending physicians/surgeons in data entry techniques
- Serves as an educational resource regarding the STS National Database for the Division of Cardiac Surgery
- Perform in-hospital outcome data collection
- Determine and utilize software applications for data collection and analysis
- Provide accurate entry of data into the program’s software and ensure transmission of completed data to regulatory agencies as required (STS, DPH)
- Establish effective working relationships with members of the surgical team, medical and nursing staff, cardiac research data staff, the medical records staff, IT staff and other services within the hospital as well as counterparts involved in data collection and reporting at community cardiac surgery site(s) whose support is necessary to the management and success of the program
- Participate in projects, meetings and committees as required
- Licensed in MA as registered nurse
- Minimum 3 years experience in inpatient surgical nursing required, 1-3 years cardiac surgery experience strongly preferred
- Computer skills and experience with MS Office products (Word, Excel, PowerPoint and Access)
- Clinical chart review and abstraction experience
- Database management experience
- Statistical knowledge
- Quality improvement or patient safety knowledge and experience
- Strong interpersonal and communication skills; able to work independently and as part of a team; able to communicate technical information such as during training
- Understanding of adult learning to facilitate training activity
- Ability to work accurately and maintain attention to detail
81
Research Nurse Resume Examples & Samples
- Recruits, screens, enrolls, and evaluates patients in the inpatient and outpatient cardiology clinics, as well as, the CVICU
- Assists the potential research participants and their families throughout the study
- Collects study specimens and checks vitals; assists with patient examinations
- Schedules the research participants’ appointments for study related tests and procedures
- Retrieve and submit all collected data to appropriate party or data coordinating center
- Tracks progress toward meeting project milestones and ensures clinical and research data is entered into databases in a timely and accurate manner
- Regulatory work including drafting, submitting, and amending new or ongoing research protocols for Institutional Review Board review
- Ensure compliance NIH, PHN, IRB, Industry Sponsors, TCH, BCM, and external institutional regulations
- Maintain records and regulatory documents
- Work effectively with the research team to ensure appropriate and high-quality cross-coverage of different protocols
- Help meet study timelines as determined by the PI
- Serves as clinical resource for other members of the multidisciplinary team
- Attends and participates in departmental education opportunities
- Performs responsibilities in a manner that promotes quality and safe patient care and customer service
82
Research Nurse Resume Examples & Samples
- Screening and enrolling subjects
- Obtaining blood and other specimens for tests, administering medications, recording data for research analysis, and maintaining patient records
- Training in phlebotomy and processing of biologic specimen
- Coordination of research activities for a Pediatric Clinical Research Program with performance of metabolic studies and clinical trials
- Recruitment and consent of research participants, submission of research protocols for regulatory agencies (IRB; research units), maintaining regulatory binders, scheduling of research visits, assisting the physician with study procedures and supervision of completion of research protocols
83
Research Nurse, RN Resume Examples & Samples
- Knowledge of research methodology, protocols and data collection methods
- Ability to develop and implement research and data collection protocols
- Knowledge of current clinical nursing practices and procedures. Particular knowledge of maternal child health nursing required
- Excellent interpersonal skills permitting effective recruitment and interaction with participants, medical and administrative staff at study sites and other study personnel
- Excellent verbal communication, including skill in making presentations and providing training
- Strong organizational skills and ability to work independently and take initiative, balance competing demands, schedule and plan efficiently and effectively to coordinate with participating clinic staff, meet participant recruitment goals and coordinate with other study personnel
- Ability to work well as a team member and to exercise discretion, judgment, tact and diplomacy
- Proficiency and skill with computer databases and software packages such as Word, Excel, Access, Power Point, Endnote, STATA and SAS
- Meticulous attention to detail and confidentiality. Knowledge of HIPAA and patient privacy regulations
- Knowledge of regulations related to the protection of human subjects, informed consent, and OSHA/blood borne pathogens
- Commitment to diversity and to serving the needs of a diverse community
- Five years experience as a registered nurse in a clinical setting
- Five years experience as a research nurse
- Five years experience recruiting and interviewing research participants or other comparable experience
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Senior Research Nurse Resume Examples & Samples
- Degree / relevant professional nursing qualification, registered on the Nursing and Midwifery Council and clinical experience
- Substantial experience of working within wound healing including research
- Able to demonstrate professional knowledge within wound healing to give advice and guidance to internal and external customers
- Possession of a full UK driving licence and access to own transport arrangements
- Evidence of ability to explore customers’ needs and adapt the service accordingly to ensure a quality service is delivered
- Proven ability to develop networks in order to contribute to long term developments
- Evidence of demonstrable knowledge of key advances within specialist discipline
- Evidence of ability to undertake and deliver specific projects and supervise short term project teams
- Experience of working in a Higher Education environment
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Research Nurse Coordinator Resume Examples & Samples
- Supervises the Clinical Regulatory team including Clinical Research Coordinators, Research Nurses, and Clinical Research Technicians
- Coordinates and implements the research studies according to the study protocol. Obtains all necessary approvals and informed consent forms; Works directly with the physician/investigator and clinic staff to ensure protocol compliance
- Identifies, screens, recruits eligible patients and enrolls patients into the study Presents trial concepts and details to the patients, and obtain informed consent when appropriate Documents informed consent process and all components of the study procedures
- Participates in ongoing patient education. Coordinates scheduling of tests and treatments required for the protocol. Maintains research patient database according to Standard Operating Procedures (SOP)
- Assesses patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to device procedure, and thoroughly documents all findings
- Ensures accurate and complete data collection, entry, and timely submission to central operations in accordance with SOPs
- Coordinates research device procurement and accountability records in accordance with SOPs
- Maintains protocol regulatory documents in compliance with SOPs. Communicates, reviews, and documents regular Regulatory Meetings with physicians and other clinic staff as appropriate
- Participates in local quality assurance program and develops appropriate action plans for quality improvement
- Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards. Maintains strict patient confidentiality according to HIPAA regulations and applicable regulations and laws
- Performs certain research procedures that include any physical interaction with the research subject by placing the study device or assisting the physician investigator with placing a study device or administering contrast agents during procedures when indicated
- Collects tissue specimens from the research subject during medical procedures (i.e. biopsies) and coordinates the acquisition and documentation of clinical and pathological findings
- 2 years of nursing experience required; Two years clinical research
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Research Nurse Resume Examples & Samples
- Screening and enrolling subjects, obtaining blood and other specimens for testing, recording data for analysis, conducting periodic home visits, clinical triage and assessment of patients, and maintaining patient records
- Recruits, screens, enrolls, and evaluates patients at study sites
- Maintains patient charts and medical records
- Instructs patients on prescribed therapeutic regimens, home care, and health maintenance
- Communicates and follows up with patients via telephone and/or EpicCare MyChart regarding clinic appointments, home visit reminders and follow ups, and answers patient questions as appropriate
- Ensures the clinical studies are conducted in accordance with protocols and the IRB. Contributes to IRB reporting and data analysis
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Research Nurse Resume Examples & Samples
- Provision of direct patient care,
- Development of care delivery systems and programs to ensure the provision of a DUHS standard of quality care at affiliated sites,
- Coordination of clinical and research services at affiliated sites,
- Effectively building relationships, facilitation and collaboration with all parties involved in with the Duke-affiliated radiation and medical oncology programs,
- Collaboration with DCN administrative, medical, and clinical nursing leadership. The nurse interacts with nursing leadership and nursing staff in affiliated hospitals in support of Duke-affiliated cancer programs and represents the interests of the Duke Cancer Network on committees, teams and other public forums
- Functions within the policies and procedures of the Duke University Health System and local affiliated oncology programs
- Demonstrate ability to read, ascertain, and disseminate relevant information from clinical protocol documents
- Knowledge of and appropriate application of the nursing process, professional theory, practice and procedures
- Certification in Clinical Research strongly recommended (SOCRA, ACRP)
- Knowledge/experience in clinical research
- Knowledge of HHS and FDA human protection regulations
- Able to independently seek out resources and work collaboratively and maintain effective working relationships
- Able to use computer and learn new software programs
- Working knowledge of the multidisciplinary management of cancer patients, procedures and techniques involved in administering chemotherapy and care of radiation oncology patients
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Clinic Research Nurse Resume Examples & Samples
- Assists with the preparation, submission and management of internal/external compliance documentation at all stages of the research project
- Assists with the selection, education, testing, and monitoring of research project participants. Follows protocols and collaborates with other healthcare providers to ensure continuity of participant care
- Documents patient care and study results using appropriate formats and systems. Communicates patient/study results on an on-going basis to research team
- Participates in quality assurance/improvement initiatives. Ensures compliance with applicable standards of care and regulatory requirements
- Minimum Requirement: Experience in Cardiac Nursing
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Research Nurse Coord Resume Examples & Samples
- Assist the Principal Investigator in feasibility and budget assessments for research studies
- Organize and maintain appropriate regulatory documents in accordance with sponsor and institutional standards throughout the life of the study
- Schedule, perform, and/or coordinate all study procedures according to protocol requirements and sponsor conventions
- Identify adverse events according to study standards; triage, report, and document with the Principal Investigator according to IRB and sponsor requirements
- Document and record, in writing or electronically, all study events and protocol related procedures
- Review and abstract medical record information in a consistent manner, in accordance with study protocol, institutional, and HIPAA requirements
- Attend meetings, conferences, and seminars as required
- Adhere to all institutional health, safety, and infections control regulations and requirements
- Adhere to the policies and procedures of any clinical site where study is being performed
- Perform additional duties as trained and required by study protocols
- RN with current registration to practice nursing in Massachusetts
- 3 years of relevant nursing experience
- Phlebotomy and EKG skills preferred
- Demonstrated Microsoft office skills
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Research Nurse Coordinator Resume Examples & Samples
- Assist in the development of research protocols, case report forms, and case report form completion guidelines
- Screen patients according to study criteria, randomize, enroll, and consent in accordance with GCP standards
- Perform nursing assessments of study participants according to protocol and consult with clinician or Principal Investigator as necessary
- In collaboration with the investigational pharmacy, ensure proper adherence to randomization schema, study drug dosing and administration per protocol
- Review clinical system billing charges for accuracy and appropriateness
- Ensure that all required study event and protocol related data is accurately and efficiently entered into the clinical trial management system
- Maintain patient/subject confidentiality and strictly adhere to all federal, state, and institutional standards for GCP
- Maintain business confidentiality as it relates to sponsor, protocol and related regulatory documents
- Attend meetings, conferences, seminars, and applicable training as required
- Ensure that all staff adhere to policies and procedures of any clinical site where study is being performed and adhere to all institutional health, safety, and infections control regulations and requirements
- Perform other duties as required
- Strong oral and written communication skills, attention to detail is essential
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Research Nurse Coord Resume Examples & Samples
- Maintain and coordinate all aspects of complex study conduct, including data and source documentation, adverse event reporting, and communications with the IRB
- Assess study budget and recommend changes and adjustments as necessary
- In collaboration with the Principal Investigator, assist in collation, writing, and editing of research results
- Maintain business confidentiality as it relates to sponsor, protocol, and related regulatory documents
- Adhere to policies and procedures of any clinical site where study is being performed
- 5 years of relevant nursing experience, 2 years of which must be research nurse coordination experience
- GCP Training
- Certification as a CCRC or CCRP preferred
- Ability to coordinate a protocol from its inception to completion and problem solve difficulties during it life cycle
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Per Diem Research Nurse Resume Examples & Samples
- Candidate must be a graduate of an accredited School of Nursing
- Currently licensed as a Registered Nurse in the Commonwealth of Massachusetts
- Requires demonstrated written and verbal communication skills
- Ability to utilize the nursing process and to work collaboratively
- No experience required; one year medical/psychiatric experience preferred
- MR safety certification
- Standard blood draw procedures (excluding IV placement)
- All employees must possess basic computer skills to use a variety of electronic or online systems for communication, clinical and administrative purposes
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Clin Research Nurse Liaison Resume Examples & Samples
- Formulate care plans (primary emphasis on nursing communication, nursing orders, parameters and administration issues) in collaboration with Investigational Pharmacist and study team
- Provides consultation to the principal investigator, infusion center, research study team or clinical nurse coordinators as it relates to clinical trial patients, protocol and research guidelines
- Patient treatment plans are routinely reviewed and compare to study protocol
- Provide direct nursing care to clinical trial participants
- Provides leadership and serves as a resource in the provision of the care and activities related to clinical research participants
- Provide patient, caregiver, and colleague education
- Conduct an annual clinical research needs assessment and uses results to construct a strategic plan to develop plans for meeting those needs
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Research Nurse Resume Examples & Samples
- Bachelor of Science in Nursing
- Good computer skills, including working knowledge of a personal computer and Microsoft Office (Word, Access, Excel, and PowerPoint) and basic statistics
- Must be able to successfully pass the Basic Windows Skill Assessment at 80% or higher rating within 30 days of employment
- Good communication, organization, and interpersonal skills
- Develops, conducts, and facilitates research protocols
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Research Nurse, Cardiology, Evanston Hospital Resume Examples & Samples
- Manage patient care within the study parameters
- Be responsible and accountable for assessing, implementing and evaluating the delivery of subject/patient care while fulfilling the daily requirements of medical research protocols
- Prepare and submit IRB documents, as required
- Work on cardiac device studies
- Research certification desirable and mandatory after 2 years in the position
- Prior experience with cardiology patients preferred
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Research Nurse Manager Resume Examples & Samples
- Baccalaureate degree required; Baccalaureate degree in nursing preferred
- Certification in Oncology Nursing, OCN, ACON, or CPON strongly preferred
- Minimum of 3-5 years oncology experience required, leadership or charge nurse experience preferred
- Experience as a clinical research nurse preferred
- Demonstrates knowledge of computer systems in use at the Institute
- Provides input into the annual budgetary process
- Participates in the Nursing Leadership on-call schedule
- Assists with development, implementation and monitoring of unit based quality improvement, safety and patient satisfaction activities that are consistent with the goals of the Department of Nursing and Patient Care Services
- Facilitates continuous quality improvement in processes and services as directed
- Serves as clinical research expert
- Coordinates and participates in unit based audits and monitoring of nursing quality indicators
- Fosters a systematic awareness of the diversity that exists within the organization including but not limited to culture, ethnicity, gender, and age, and promotes an environment that is sensitive to the diverse patient populations
- Complies with the accepted standards of professional nursing and research practice, as well as with all licensure/registration requirements applicable to the nursing role
- Critical thinking, collaboration and excellent communication skills
- Thorough understanding of cancer disease process and treatment
- Knowledge of scientific principles and clinical research methodology
- Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other groups as protected by law
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Research Nurse Resume Examples & Samples
- Delivering a brief, structured educational intervention per study protocol
- Meeting with families in a busy outpatient medical clinic setting for intervention delivery
- Completing study-related documentation in electronic medical record and study databases
- Meeting regularly with study team
- Completing all required training modules related to the Responsible Conduct of Research (e.g., CITI Program training)
- Evening and weekend telephone calls or meetings with study participants may be needed on occasion
- Trained in skills and information relevant to behavioral diabetes research, including: - Learning the relevant aspects of the study protocol, including being trained in the structured delivery of the study-related intervention - Learning to complete required compliance-related documentation for behavioral research
- The individual is expected to be highly organized, keep detailed records, and display good verbal, communication, and problem-solving skills
- Respectful, patient-centered interactions with participants, medical providers, and staff are expected at all times
- Research activities will potentially take place at any of the TCH/BCM locations in the Houston metro area in which diabetes care is provided
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Research Nurse Resume Examples & Samples
- Participate in protocol development by drafting study protocols and/or reviewing potential protocols to evaluate their effect on standard nursing procedures; Submit to Human Subjects Committee and Scientific Review Committee for approval
- Recruit study participants by referrals or by placing advertisements on television, radio or in newspapers; Schedule appointments, interview and evaluate potential participants to ensure they meet eligibility requirements; Instruct participants concerning protocol and obtain consent signature
- Schedule and/or coordinate the scheduling of required laboratory tests, patient visits, and/or exams
- Provide direct patient care involving diagnosis, administering medication and performing tests using specialized Dermatology equipment to included but not limited to confocal microscope and skin cancer testing
- Coordinate and/or perform physical assessments required by protocol such as tumor measurements and skin checks
- Evaluate and develop patient educational materials and give patient and/or family members instructions on drug administration and other medical information
- Prepare financial records including quarterly reports, budget and patient related expenses
- Maintain close communication with the assigned finance officer for each specific project
- Assess participants for evidence of drug toxicity, unexpected side effects or other problems and notify principal investigator; Recommend dosage adjustments
- Assist physician and/or principal investigator in writing manuscripts for publication and/or presentation of materials at conferences; Assist in the preparation of NIH, NCI, and PPG grants
- Inventory and requisition supplies and equipment; Arrange for repair and maintenance of equipment
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Research Nurse, Hem / Onc Resume Examples & Samples
- Two or more years of pediactric clinical experience OR four or more years of clinical related experience
- Bachelor of Science in Nursing
- Experience in the subspeciality of involvement
- 1 year of experience in research with knowledge about the conduct of clinical trials, research principles/methodologies, and study design
- Pediatric Advanced Life Support (PALS)
- Working knowledge of federal regulations and regulatory requirements for conducting research
- Good computer skills, including working knowledge of a personal computer and Microsoft Office (Word, Access, Excel, and PowerPoint) and basic statistics
- Must be able to successfully pass the Basic Windows Skill Assessment at 80% or higher rating within 30 days of employment
- Self-directed and motivated to work independently toward short- and long-term goals
- Good communication, organization, and interpersonal skills
- Develops, conducts, and facilitates research protocols
- Performs quality and education activities
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Research Nurse Resume Examples & Samples
- Ensures initial and ongoing consent process is performed and documented in compliance with the U.S. Food and Drug Administration (FDA), Good Clinical Practice, institutional policies, sponsor requirements, Institutional Review Board (IRB) and other applicable regulations, guidelines and policies
- Collaborates with Principal Investigator (PI) to ascertain study patient eligibility for a clinical trial, including documentation of criteria specified in the protocol. Identifies and develops processes to overcome recruitment barriers
- Interfaces with the Office of Grants and Contracts (OGC) and IRB to ensure all documents are processed and maintained per applicable regulations
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Research Nurse Resume Examples & Samples
- CA licensure as Registered Nurse (RN): Possession of the legal requirements to practice as a Registered Nurse as determined by the California Board of Registered Nursing
- CA Driver’s License
- Six months of (in last five years) clinical nursing experience in oncology
- Excellent interviewing skills
- Basic computer skills (i.e. e-mail, Word, Excel)
- Excellent organizational skills and attention to detail
- Able to drive to research sites and participants’ homes in the greater Bay Area
- Venipuncture skills
- MSN degree in Nursing or equivalent in education and experience
- Experience enrolling patients in research study and implementing a research protocol
- Experience using SPSS for data entry
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Research Nurse Coordinator Resume Examples & Samples
- BS in Nursing
- Minimum of 1-2 years nursing experience, to include a combination of the following: - Pediatric experience - Research experience
- Pediatric phlebotomy skills
- Current Washington State licensure to practice nursing
- As a condition of employment: Current BLS for Health Care Providers is to be maintained at all times by all nurses. Note: current PALS and/or PEARS will be accepted in lieu of BLS, and must be maintained as current at all times. Employees are responsible for any costs (including time away from work) associated with obtaining PALS or PEARS certification if it is not a requirement of the position. (ACLS will not be accepted as a substitute to the requirements listed above.)
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Research Nurse Resume Examples & Samples
- Assist with collection of data for clinical research protocol visits conducted with out of town subjects. This may include obtaining medical history and/or questionnaires, administering allergy skin tests, blood drawing, pulmonary function tests, assessing blood pressure and pulse, and instructing in and demonstrating the use of equipment and/or procedures to be used by participants
- Maintain accurate and detailed records in accordance with Federal Regulations as well as study protocols. This includes administration of and maintenance of consent documents, questionnaires, screening of medical tests for abnormalities, regulatory binder documents, sponsor and other regulatory binder documents. Responsible for taking appropriate actions to inform subjects and/or investigators when appropriate
- Assess eligibility for recruitment by contacting, scheduling, and screening potential participants using various questionnaires and/or medical tests. This requires intense persistence in maintaining contact with participants, and may require occasional evening or weekend hours
- Inventory of equipment and supplies in accordance with study protocols to insure no expired items are used, to insure all equipment is functional and calibrated, and to insure all records or logs are maintained as required
- Written and verbal fluency in English and Spanish
- Direct Experience in Human Subjects Research
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Research Nurse Clinician Resume Examples & Samples
- Graduate of an accredited school of nursing with a license to practice in the State of New Jersey
- One (1) year of oncology experience required
- Must maintain active Basic Life Support (BLS) certification
- The ideal candidate will be detail oriented, have excellent organizational skills, be proficient in computer applications (Oncore™, Word, Excel, etc.), possess excellent communication and interpersonal skills, be able to maximize resources and be resourceful
- Equivalent education, experience and/or training may be substituted for the degree requirement
- Three (3) to five (5) years of oncology research experience preferred
- Oncology Nursing Society (ONS), certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN) is preferred
- Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP),is preferred
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Research Nurse Resume Examples & Samples
- Interview, screen and recruit patients for entry into protocol; contribute to conferences determining who will be accepted into the UDP
- Determine suitability of patients for travel
- Communicate with families and caregivers to obtain medical records; conduct family interviews to obtain comprehensive understanding of the care needs of the patient and family members during travel to and from the NIH and throughout the evaluation period
- Serve as point of contact for families and their physicians; perform data retrieval; communicate test results to outside entities; ensure adequate consents
- Respond to phone calls from patients or potential patients inquiring about specific diseases
- Adjust patient’ plan of care in the absence of established guidelines
- Work with Principal Investigator to make recommendations to patients and families regarding disease management
- Develop new standards for novel and unpredicted research situations and interventions
- Provide on-call services to the multidisciplinary team, relevant to all matters of clinical research issues, for patients who are seen on-site
- Provide mentorship to nurse specialists to develop skills and expertise in program areas
- Provide in-services to inpatient and outpatient unit nursing staff; provide informal education to care providers
- Direct health care members in the execution of trials and resolution of logistical constraints; ensure that all aspects of Good Clinical Practice (GCP) and federal regulatory requirements are met/exceeded
- Design, implement and evaluate complex protocols; manage challenging patient populations
- Develop intake tools and screening forms; work with staff on the general administration of protocols’ implementation
- Serve as liaison between NIH and various outside agencies to further the mission of education and protocol implementation
- Initiate active efforts for protocol enrollment
- Collaborate with staff to obtain and maintain informed consent/assent and address ethical and legal implication of same
- Direct and perform quality assurance and quality control activities relating to protocol adherence, protocol monitoring, data collection, data abstraction and data analysis
- Ensure that standard operating procedures (SOPs) reflect the highest standard of rigor
- Manage data through Labmatrix, CIT, CRIS and UDPICS databases to ensure accurate and reliable data entry
- Perform and/or coordinate the collection, processing and handling of laboratory samples, including appropriate storage and shipping
- Serve as point of contact among laboratory personnel, families and phlebotomy services to ensure timely acquisition and receipt of samples
- Engage in team meetings to update team members of changing directions in study implementation
- Report data to appropriate regulatory and monitoring agencies; anticipate and create databases and data capture forms to meet protocol needs
- Facilitate the ease of reporting, avoidance of repetition of data entry procedures and generation of reports appropriate to various agencies
- Design and maintain a selection of materials appropriate to send to health care referral sources seeking eligibility information or other objectives
- Perform data searches of medical records for analyses of patient characteristics
- Survey the medical literature for background information on specific aspects of the diseases under purview
- Problem-solve complex or unpredictable situations and improve processes and services to patients and colleagues
- Participate in clinical practice and research support meetings; develop multidisciplinary performance improvement programs and projects
- Collaborate with staff to analyze and evaluate current systems of health care delivery and to identify and implement new practice patterns
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Research Nurse Resume Examples & Samples
- Recruits, screens, enrolls and evaluate patients that participate in a research study
- Schedules study visits and meetings related to studies
- Collects study specimens and check subjects’ vital signs
- Administer study medications
- Follow subjects’ progress and advises the Principal Investigator
- Ensures the clinical studies are conducted in accordance with guidelines of the FDA and other regulatory agencies
- Educates patients in significant aspects of study
- Serves as a liaison and distributes research information to faculty, research staff, principle investigator, and others as required
- May assist in developing the clinical trial agreement
- Maintains clean and safe work environment
- Stocks and orders supplies
- Provides training and guidance to research nurses and other research personnel and serves as a resource to staff
- Performs other job related duties as assigned
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Research Nurse Resume Examples & Samples
- Self-directed and organized
- Experience with computer spreadsheets & database management
- Excellent phlebotomy skills (adult and pediatric preferred)
- Team player and with good interpersonal skills
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Research Nurse Resume Examples & Samples
- Coordinates and ensures accurate protocol implementation and conduct for all assigned protocols
- Registers all patients, obtains and maintains randomization and dose levels; maintains records of patient accrual by protocol as required
- Completes case-report forms and performs quality assurance checks on all data (in coordination with the QA/QC Manager)
- Acts as liaison with drug companies or sponsoring institutions
- Coordinates with ICTR Regulatory Affairs the completion of required actions as directed by the drug company or other sponsored agency
- Coordinates IRB interactions (in conjunction with ICTR regulatory affairs)
- Coordinates all care for patients enrolled on assigned protocols to ensure that the study is implemented as it is written and that all required data are available and collected
- Assists Principal Investigator with informed consent
- Coordinates all treatments and tests with inpatient and outpatient staff; requests or assists with scheduling and ensures results are received
- Coordinates Affiliate involvement with study conduct, Investigational Pharmacy, Research Office, Diagnostics, Credentialing, etc., as needed
- Ensures research needs are met at all patient/family meetings (discuss progress of treatment, changes in therapy, etc.)
- Acts as liaison between patient and PI/MD concerning problems, adverse reactions, and other patient care issues as they may relate to the study drug
- Follow-up with patients during each study visit to answer questions and assess for any toxicities or side effects
- Maintain effective communication with patients, physicians, and the company representative or clinical monitor for each research protocol
- Serve as consultant and provide assistance to nurses, fellows and professional staff for education on specific ongoing research projects to include investigational drugs, devices, or procedures
- Perform study specific procedures (i.e. blood draws, education, investigational product administration and accountability, and administer questionnaires)
- Ability to effectively communicate with patients, families, physicians, and other healthcare providers
- An in-depth working knowledge of IRB requirements, FDA regulations, Good Clinical Practice, and ICH guidelines for the conduct of clinical trials
- Must be conscientious, detail-oriented and be able to effectively manage multiple priorities concurrently
- Possess tact, discretion and independent judgment
- Inspired by the potential for improvement; should be able to work independently and to accept direction and guidance
- Experience working in a team environment and comfortable working in areas such as the cardiac catheterization lab, operating room, and radiology
- Proper utilization of medical equipment and supplies, and experience with specimen processing
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Research Nurse Specialist Resume Examples & Samples
- Knowledge and understanding of the Vanderbilt policies and regulations governing the protection of human subjects
- Has a working knowledge of the operations of the Vanderbilt Institutional Review Board and its requirements for the protection of human subjects
- Maintains a clear understanding of the Federal regulations governing the protection of human subjects, e.g., FDA, OHRP, GCP/ICH guidelines, and HiPAA regulations
- Understands, implements and follows a clinical study protocol and is able to conduct multiple studies independently, including accurate data collection (able to identify when training is needed to safely and accurately perform or assess required procedures. Problem solves when needed to acquire or deliver such training)
- Independently prepares and stores critical documents required to be maintained and provided to the sponsor during and after the conduct of a clinical trial
- Participates in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation and research procedures
- Participates in the determination of eligibility and recruits candidates for study participation. Strives to ensure studies are completed in a timely manner through implementing effective screening and recruitment strategies and completing required documentation in an accurate and timely manner
- Provides education and training to appropriate personnel and participants in research specific methodology and procedures
- Maintains open and positive communications with investigators, participants, co-workers, other departments and sponsors. Collaborates with other departments to seek solutions to global research concerns
- Ability to multi-task, managing multiple assignments while maintaining documentation and study visits and procedures in a timely manner
- Digests complex clinical information to determine if documentation is accurate, complete, and to ensure procedures contain appropriate safeguards. Understands standard of care versus research and continually assesses need for additional protections for the protection of research participants and the appropriateness of research data
- Utilizes nursing skills and processes to identify participant and study problems, and utilizes problem solving skills to identify solutions following through to implement solutions and assuring goals are met
- Proactively involved in quality improvement through ongoing assessment and through the identification of issues and planning and evaluation of quality improvement
- Assists in budget and contract negotiation and facilitates interactions between sponsors and institutional departments
- Reviews the Research Support Services website to obtain information regarding available and required in-services, required certifications and to obtain important updates
- Attends the Clinical Research Staff Council and participates in CRSC activities
- Attends in-services advertised by the Institutional Review Board, Research Support Services, professional societies, etc
- Demonstrates initiative in self-directed learning, as evidenced by attendance of professional development opportunities. Actively seeks new learning opportunities. Sees learning as part of work
- Assumes responsibility for continuous learning, engaging in a minimum of 15 hours of educational activities annually or pursuing an advanced academic education or certifications
- Clinical research experience preferred but not required
- Knowledge with cancer patient population
- Experience with Excel, Word, and Star Panel preferred
- Experience working in a collaborative environment
- Strong written and oral communication
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Rn-clin Research Nurse Resume Examples & Samples
- Demonstrated knowledge of medical terminology
- Demonstrated knowledge of FDA and OHRP HIPAA policies
- Working knowledge of computer applications including MS Office and RedCap
- Knowledge of behavioral protocols for weight loss
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Research Nurse Resume Examples & Samples
- Basic computer operation skills (keyboard and mouse use, Internet browser use, opening and closing programs)
- Able to process e-mail (read, send, delete, file)
- Computer skills in word processing, database management, and spreadsheet applications beneficial Continuing education in a research related field beneficial
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Research Nurse Resume Examples & Samples
- Knowledge of patient care standards and practices normally acquired through completion of a Bachelor's Degree in Nursing or an agreement to pursue
- Possesses an active Wisconsin RN nursing license
- Current CPR certification or obtained within 90 days of hire
- Oncology Nurse Certification preferred (OCN) or obtains within 18 months of hire
- Possesses and maintains a valid Wisconsin Driver's License required
- A minimum of two years' acute care oncology nursing necessary to enhance and develop skills
- Previous outpatient clinic and data management experience beneficial
- Clinical Research experience desired but will train candidate with strong oncology nurse background
- A general understanding of peer review processes, familiarity and knowledge of medical & research records organization and procedures, and ethical commitment to the confidentiality of all data and information
- Proficient computer skills and familiarity with EMR documentation in EPIC
- Public speaking skills, the ability to write clear and legible clinical notes, and the ability to interrelate with physicians, nurses, managers and other hospital personnel necessary to communicate with a wide variety of individuals
- The ability to organize and prioritize time while functioning under limited supervision and possess the ability to pay close attention to detail
- Good public relations skills necessary to coordinate multiple assignments
- Interviewing skills and the ability to collect data, analyze information and assist with recommendations and implementation of policies and procedures necessary to perform research duties
113
Research Nurse Per Diem Resume Examples & Samples
- Participates as a member of the research team in the coordination and delivery of care to oncology patients participating in clinical research protocols
- Reviews all clinical study records, including informed consents, to ensure complete study documentation in compliance with regulations
- Manages patient care under the supervision of the attending MD to include symptom identification, symptom management, and follow-up medical care
- Triages patient calls appropriately and consults with the attending physician when needed or requested
- Maintains management and oversight of patients being treated on assigned clinical research protocols
- Provides feedback to members of the management team in the development of policies and procedures as requested
- Performs record abstraction to obtain eligibility and inclusion/exclusion criteria for patients in consideration for entry onto research studies
- Completes all necessary paperwork required for serious adverse event reporting
- Assists research staff in preparing for monitoring visits. Meets with monitors when requested or needed
- Provides care to patients including but not limited to peripheral lab draws, central line draws/care, and EKGs
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Research Nurse Coord Ii-neurology Resume Examples & Samples
- Assist the Principal Investigator in feasibility and budget assessments for research studies, recommend changes and adjustments as necessary
- Responsible for the protocol specific training of the study team and clinical staff
- Provide feasibility assessment of research study protocol requirements and design a recruitment plan for assigned clinical studies
- Participate in Quality Assurance internal audits
- Take primary responsibility for creation and maintenance of all regulatory documents, including initial IRB submission, continuing review submissions, and FDA and sponsor required regulatory documents
- Responsible for all regulatory paperwork and to report findings to the Principal Investigator, sponsor, and IRB when necessary
- 5 years of relevant nursing experience, 2 years of which must be research nurse coordinator experience
- Proficiency in electronic medical records and relevant computer software
- Ability to work in a team environment to facilitate the integrity of the study and its timely completion
- Ability to travel to off-site locations
- Experience with OnCore and Epic
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Research Nurse Resume Examples & Samples
- Serve as nurse health educator for Center projects. Deliver protocol driven health education interventions to study participants (via face-to-face, telephone or videoconferencing technology as appropriate). Schedule and coordinate sessions, attend and participate in supervision sessions, records sessions as directed, and perform health educator data collection during initial visit and follow sessions. Train study participants on key elements of the study protocol. Monitor study participant adherence to key elements of the study protocol. Perform nursing duties as needed including phlebotomy tasks, case management, and clinical decision-making
- Working collaboratively with other Center personnel to achieve the goals of funded studies at the Center. Serve as liaison to physician, nurses, and staff in the study clinics to ensure smooth running of research projects. Track and monitor adverse patient outcomes
- Serve as community liaison for the Center. Provide health education to community sites, establish community partnerships and work with designated community sites to advance the research, education and training mission of the Center
- Supervise summer student trainees at the Center. Work with summer students (including, high school, college and medical students) during their summer experience. Assist with data collection, data entry, and provide guidance on research related issues
- Perform statistical analyses with SAS/STATA/SPSS and prepare abstracts, posters and presentations for scientific meetings
- Coordinate multiple active grants at the Center for Patient Care and Outcome Research as needed with tasks to include recruiting study participants, data entry/cleaning, and coordinating IRB submissions and renewals. Compile and maintain research files, grant files and related records and serve as liaison between funding agencies, institution administrators, and researchers. Other Duties as assigned
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Research Nurse Resume Examples & Samples
- Coordinate, evaluate and follow patient participation in clinical research. This includes, but is not limited to identifying, enrolling and consenting patients, organizing study visits and follow-ups, responding to patient telephone calls
- Assist in the collection and evaluation of data. Complete all forms required for proper protocol documentation. Enter patient data into database and other programs. Maintain patient records
- Under physician direction, perform protocol-specific clinical tasks including patient assessment, screening, ordering tests, collecting specimens, and monitoring responses. May administer medication or other types of protocol specific intervention
- Identify problems or obstacles in the system/procedures related to implementation of the research protocols and data collection, and communicate to the study investigators. Notify appropriate personnel of any complications or untoward effects of research
- Provide patient and family education. May provide staff education concerning research protocols as required
- Assist with the development, implementation and monitoring of QI activities. Implement and conduct quality control processes to ensure the highest data standards. Develop clinical review data review plan and edit check specifications
- Assist in the writing and submission of IRB protocols, grant applications, and consent forms. Conduct literature searches. Assure compliance with all relevant IRB and other regulatory agency requirements
- Maintain and manage data and data systems supporting research activities. This includes correspondence with IRBs; forms and data entry and cross-checks; development and maintenance of computerized record systems to track and account for patient’s participation
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Supv, Research Nurse Leukemia Resume Examples & Samples
- Personnel
- Data Management
- Audit
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Pd-research Nurse Resume Examples & Samples
- Assist in reviewing literature and research material for publication
- Counseling subjects for HIV/AIDS and testing if requested
- Act as advocate and liaison between Spanish and other non-English speaking subjects with MDs and staff
- Oversee and manage all surgical and medical equipment and sterilization process
- Perform patient general, physical and gynecological examinations (including PAPs, STD screenings, wet mount and office microscopic examination of patient vaginal discharge samples)
- Assist MD in reviewing and analyzing of all subject lab work and results. Manage the office and relevant aspects in the absence of the office manager. Assist MD with patients exams and related office surgical procedures
- Attend to and assist monitors and regulators during office site visits. Collect, prepare and deliver to labs all subject required lab work
- Responsible for timely case report forms corrections via queries system
- Do all phlebotomy activities including starting IV lines and administering of medications under MD supervision during operational medical procedures, when protocol requires
- Follow subjects to ensure compliance with protocol standards and maintain ongoing communication to improve enrollment and retentions in the studies
- Responsible for consenting subjects and for ensuring that subjects are fully informed of the consent process in their own native language. Responsible for all subjects charts and case report forms and computer submissions
- Meet with Principal Investigators, Coordinators and research staff for procedural discussions relating to studies protocol, inclusion/exclusion and other criteria
- Coordinate the recruitment and interviewing of research subjects. Assist with IRB initial and follow-up applications and correspondence
- Assist in the organization and implementation of investigational studies
- To qualify you must have a NYS RN License with current registration
- Bachelors Degree in Nursing, or equivalent combination of education and experience with plans to earn a Baccalaureate degree in Nursing
- Experience working with specific indications (department-specific)
- Minimum of 3 years progressively responsible related experience coordinating clinical/research trials studies
- Proficiency in using various Microsoft Office applications such as World, Excel, Access, PowerPoint and Outlook
- Familiar with Internet applications
- Effective verbal and written communication skills and strong analytical, organizational and interpersonal skills
- Ability to interface effectively with all levels of management and work and communicate effectively with both internal and external customers
- Ability to work within a team environment, as well as independently
- Ability to manage time, multi task and prioritize work
- Ability to identify, analyze and solve problems
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Research Nurse Resume Examples & Samples
- May orient and train clerical staff regarding many aspects of carrying out the initial patient screening and subject recruitment protocol; scheduling of initial visits and other essential duties. May (if proper training has occurred) perform EKG and or take vital signs. May be required to travel to study initiation (that is, where sponsor teaches protocol to PI and CRC)
- Employee must also complete Standard Precautions and required IRB/HIPPA tutorial. May complete assessments on study subjects/patients per protocol (with proper training); continue to follow-through with items and patients as part of research study
- Collect, prepare, ship, and/or store biological materials using universal precautions. Environmental training is provided for the proper handling and collection of biological substances and the packaging and shipment of samples
- Secure accurate signatures and forward documents and/or forms to appropriate destination. Maintains files in an organized and up-to-date manner in order to facilitate their retrieval and maintains copies of all required on-going documentation and forms for the files
- Responsible for developing in conjunction with the team recruitment strategies (i.e., analysis of annual numbers of new consults, seek out protocols for the available patient population). Maintain complete, accurate subject charts, case report forms, enrollment logs, and hospital records from patient screening through final follow-up
- Write template-defined progress notes that reflect study procedures. Participate in weekly Feasibility Meetings by presenting Protocols from disease group. Aware of study regulatory statuses for Protocols
- Utilize available resources and established procedures to identify problems for quick resolution. Conduct study visits, obtain and document information within the time frame specified
- Demonstrate knowledge of policies and procedures of the host institution where the study is being conducted and the regulatory requirements such as IRB and other approvals if necessaryudy
- Collaborate with various personnel that may be involved in assisting with specific aspects in the study
- Interact with patient/subject and families in a courteous and professional manner. Be consistent and regularly follow through with your patient/subjects reminding them of visits and compliance
- Assist with the informed consent process and ensure that the patient/subject fully understands what is required of them throughout the study
- Thorough knowledge of research study, study rationale, study subject, and clinical procedures associated with the study
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Research Nurse Resume Examples & Samples
- Informs co-workers, by posting or dialogue, of educational programs relevant to the studies ongoing on the Clinical Research Center.Upholds the ethical and moral codes of the health professionals in the maintenance of patient privacy and confidentiality. Practices under the belief in the individual dignity and health rights of every human being
- Professional Development/Education -Attends related educational programs as well as informal seminars to meet individual learning needs and interest.Actively participates in Clinical Research Centers principal investigator lectures based on upcoming or current protocols.Supports or participates in nursing research
- Upon completion of assignment, offers assistance, as needed, to other team members involved in patient care tasks.Performs accurate and safe procedures within the scope of the research nurse. Assesses patient and family educational needs and provide teaching about the informed consent process, protocol intervention procedures and its relationship to the disease process.Maintain patient rights and confidentiality with attention to safety concerns for th epatient
- Demonstrates the ability to assess situations and make critical decisions affecting research procedures.Works with fellow staff members in a team approach to help meet patient/protocol needs, communicating patient problems and progress to all members of the tea.Administer stock medication safely and withy knowledge of hospital policy and procedures
- Procedures and Nursing Skills – Plans and coordinates care based on both patient and protocol needs; reviews each protocol prior to patient admission or outpatient visit and addresses any questions or concerns to the appropriate person. (e.g., Nurse Manager, Assistant Nurse Manager, Principal Investigator). Accurately transcribes physician treatment plans and orders and Identifies short- and long-term goals and expected outcomes of patient needs and protocol requirements; sets priorities based on each
- Regularly reviews the protocol to insure that the protocol needs are being fulfilled. Prepares chart for discharge and maintainance and directs the physician in the completion of the discharge summary and other documentation as per center/hospital policy and procedure. Completes nursing discharge summary and provides for or directs the patient/family in obtaining the necessary equipment and/or medication needed upon discharge; instructs the patient/family in the steps necessary for adequate medical follow-up and/or additional hospitalizations. Maintains a copy of patient records care plan, flow sheets, protocol consent, laboratory values, etc. according to hospital policy, NIH and industry requirements
- Documents accurately and promptly nursing interventions and plan of care in accordance with center, hospital, and protocol policy; daily documents nursing assessment in patients chart; accurately records medication given, treatment rendered, and other nursing interventions. Promptly notifies the Assistant Nurse manager or Nurse Manager about any difficulties that might arise while conducting the protocol requirements and documents
- Initiates and/or completes data records relating to specific specimen collection required by the protocol. Assesses safety needs of patients and provides such according to center/hospital policy. Continually evaluates and re-evaluates nursing intervention and expected outcomes; updates nursing care plans on an ongoing basis; evaluates patient response to the protocol and to nursing and medical intervention
- Observes changes in patients status and responds promptly and with reasonable judgment. Alerting the Prinicipal Investigator and/or Nurse Manager. Administers medications safely and with knowledge of cause and effect as well as hospital protocol policy and procedure; accurately and safely performs procedures within the scope and practice of the Clinical Research Center (serial specimen collections, routine endocrine testing, administration of blood and blood products, intravenous insertion for both fluid delivery and research medication and venous access, monitoring of vital signs and adverse events)
- Provides direct care to the research patient utilizing the nursing process, formulating a nursing diagnosis with knowledge within the scope and methodology of the research protocol
- To qualify you must have a NYS RN License with current registration. Graduate of an accredited nursing program
- Bachelors Degree in Nursing, or equivalent combination of education and experience with plans to earn a baccalaureate degree in Nursing
- Prior RN experience in a clinical setting preferred
- Proficiency in using various Microsoft Office applications such as World, Excel, Access, Power Point and Outlook
- Effective verbal and written communication skills, and strong analytical, organizational and interpersonal skills
- Ability to work within a team environment as well as independently
- Commitment to continuous learning as required by department administration
- Ability to make decisions independently
- Ability to identify, analyze and solve problems; ability to work well under pressure
- Registered Nurse License-NYS
- Bachelors Degree in Nursing is highly preferred
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Research Nurse Resume Examples & Samples
- Provides support to Clinical Trials Director, Research Director and peer research coordinators on clinical trials and other clinical research-related tasks
- Participate in research-related meetings, e.g. Study Coordinator and Investigator meetings
- Devise and implement recruitment strategies
- Screen and enroll patients for inclusion in epilepsy drug/device trials
- Prepares IBRA and SPA grant forms, reports and budgets
- Responsible for data collection, regulatory documents and implementation of research protocols
- Coordinate each trial in collaboration with Sponsors, Contract Research Organizations, NYU Institutional Review Boards, NYU Office of Clinical Trials and the FDA
- Complete human research subjects protection training, HIPAA compliance certifications and all other research-related trainings and certifications
- Maintains Behavioral Standards
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Research Nurse Manager Resume Examples & Samples
- Create and implement policies and procedures to ensure operational standardization
- Build and sustain relationships with internal and external stakeholders and support the strategic plan for the organization and for clinical research
- Support departmental implementation of new technology
- Effectively communicate (written & oral) across the organization. Communicate and escalate unresolved issues at the appropriate time to the appropriate level of management
- Ensure high quality source documentation is provided to the Data Coordination Unit according to ICH-GCP guidelines providing recommendations for corrective action when necessary
- Provide coverage as needed for Research Nurses and Clinical Coordinators
- Meet regularly with disease program leaders, investigators and Research Nurse Managers/CTO Leadership to provide necessary updates
- Identify and initiate improvements, tools, processes, and forms to enhance the efficiency and the quality of work
- Provides input in the development of CTO Policies and Procedures
- Collaborates with the Senior Director of Nursing, Administrative and Medical Director of the Clinical Trials Office to manage and document performance improvement projects
- Support efforts to recruit and maintain an adequate number of competent staff to conduct clinical research in compliance with all regulatory, institutional and departmental requirements
- Responsible for the orientation, ongoing training and development of Research Nurses and Clinical Research Coordinators. Maintains an orientation and ongoing training program for CCU staff
- Collaborate with human resources to provide counseling or performance improvement of staff as needed. Responsible for tracking the current status of certifications and any required competencies
- Manage and lead staff to develop collaborative working relationships within the cancer center and with other departments as applicable. Act as a liaison with the Epic team, investigational pharmacy, Disease Management Group faculty leaders, labs, and other units of the Clinical Trials Office in an effort to maintain efficient operations of the CCU
- Conduct regular research meetings with CCU staff ensuring they are appropriately trained on new or changed policies and procedures mandated by the Perlmutter Cancer Center Clinical Trials Office
- Develop standard operating procedures in collaboration with the Clinical Trials Office Quality Assurance Unit
- Regularly advise and report on status of staffing within the unit using data collected through feasibility assessments to project staffing needs
- Responsible for the oversight of mission critical projects, including enhancement of the protocol acuity scoring system and creation of a cancer center wide clinical trial screening program for subject recruitment purposes
- To qualify you must have a NYS RN License
- Graduate of an accredited nursing program
- Bachelor’s Degree in Nursing, or equivalent combination of education and experience with plans to earn a baccalaureate degree in Nursing
- 10 years nursing experience (at least 3 years in oncology)
- 3+ years Clinical Research Experience
- ACRP OR SOCRA certification preferred
- Basic computer skills including the use of EMR and/or scheduling software
- Ability to work with diverse groups of people
- Ability to work under pressure and with a large degree of accountability
- Experience in change management, creative leadership and program development
- Demonstrates strong communication and collaboration skills to foster an effective partnership with faculty, staff and both internal and external stakeholders
- Demonstrates a high level of knowledge in oncology and clinical research and utilizes advanced leadership skills to meet the Perlmutter Cancer Centers Clinical Trials Offices mission
- Commitment to team problem solving approach using a research and patient-focused model
- Ability to multi-task and prioritize in a fast-paced environment
- Organizational skills both to function independently and as a member of a professional team
- Ability to read, understand, and follow written and oral instruction
- Excellent written and oral communication skills that enable effective relationships with patients, faculty and staff
- Excellent judgment skills as reflected in the making of appropriate decisions with consistency
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Research Nurse Resume Examples & Samples
- Facilitates recruitment to cancer clinical trials by screening scheduled patients for basic eligibility criteria. Ensures patients are informed of available clinical trials
- Provide direct patient care as part of a multidisciplinary team utilizing a base of knowledge and an understanding of the objectives of the protocol to provide continuity of care to patients throughout various stages of treatment on protocol and follow-up. Performs procedures within the scope of the NYULMC nursing practice (vital sign monitoring, specimen collection, serial blood drawing via venipuncture or venous and central access intravenous lines, fluid delivery, and assisting with medical procedures)
- Facilitates the informed consent process and evaluates patient eligibility for participation in a cancer research study with the principal investigator
- Documents study assessments, provides education and maintains communication with the research study participants and their families
- Uses expert nursing judgment to maintain the integrity of the research protocol in accordance with federal regulation and good clinical practice (GCP) guidelines, and coordinates care to ensure the compliant conduct of the trial while maintaining patient safety
- Reviews each new protocol with the principal investigator prior to approval by the peer review committee for feasibility and addresses questions or concerns to the appropriate personnel (Principal Investigator, Clinical trials Office (CTO), Medical Director, Director of Nursing)
- Participates in multi-disciplinary discussions to discuss feasibility of new protocols at Disease Management Group meetings
- Communicates effectively with all members of the research care team and with the Clinical Trials Office (CTO) throughout the study start up and closure process
- Ensures data integrity by ensuring high quality source documentation is recorded within the electronic medical record and any other research related documents
- Participates in an orientation program (Cancer Center competencies) and staff development programs relevant to clinical specialty and studies. Participates in all study-related conferences, as assigned
- Participates in performance improvement initiatives in the Cancer Center, such as work redesign initiatives, audits of departmental studies, and related work. Utilizes evidence-based practice methods to improve patient care. Follows Good Clinical Practice guidelines and federal regulations (IHC, April 1996)
- NYS RN License with current registration
- Bachelors of Science Degree in Nursing (BSN) required
- Experience coordinating clinical/research trials studies preferred
- Ability to interface effectively with all levels of staff and management
- Ability to work within a team environment as well as independently. Commitment to continuous learning
- Ability to manage time, multi task and prioritize work. Ability to identify, analyze and solve problems; ability to work well under pressure
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Research Nurse Resume Examples & Samples
- Recruit and follow patients for clinical and basic research studies on HIV vaccines and emerging/re-emerging vaccines
- Review charts to collect relevant clinical data such as laboratory test results and social background
- Interview patients to obtain medical history, sexual history, medication history, history of use of substances such as alcohol and recreational drugs, previous HIV related risks factors and history of participation in other clinical research
- Interpret data, responsible for recognizing results that merit prompt clinical action
- Perform physical assessments of patients, analyzes trends in patient conditions, and suggests possible alterations in treatment regimens according to research protocols
- Perform protocol activities such as, study drug administration, data collection and submission, patient counseling, and physical assessment
- Interpret clinical data in terms which may be understood by the patient, as well as, interpretation at a level which is conversant with other health professional including physicians
- Coordinate and ensure the collection of specimens needed for all studies on patients enrolled in vaccine studies
- Maintain contact with patients and referring physicians to explain patient’s conditions and symptoms, interprets results of laboratory tests; discusses the future status of patients who have participated in the study
- Follow up on patients throughout study to schedule procedures, follow-up examination, transportation and admissions
- Skillfully counsels patients regarding the potential risks of clinical research and obtains informed consent
- Provide competent HIV Testing & Counseling, and on occasion, deliver HIV Positive results in case of a new HIV Infection
- Participate in recruitment and outreach activities & contributes to recruitment strategies through innovative ideas
- Participate and coordinate protocol training and mentors new staff
- Enter/extract patient information to generate reports
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Research Nurse Coordinator Resume Examples & Samples
- Create and maintain study logs for effective trial management and troubleshoot patient management problems/scheduling conflicts
- Provide oversight of database content and manage large data sets produced by external contracted sources
- Assign and monitor research activities of project staff for successful and timely execution of activities in order to achieve the study and principal investigator goals
- Plan, assign and oversee work assignments for staff working on assigned project(s)
- Interact with physicians seeing patients in the clinic to assure that project requirements for patient visits are achieved
- Evaluate study participants for inclusion into study protocol by evaluating each aspect of their medical history
- Preparation and attendance of monitoring visits by the designated sponsored Clinical Research Officer (CRO)
- Comply with Good Clinical Practice Guidelines and FDA Guidelines regarding clinical research
- Ensure participants fully understand the purpose, goals, requirements of the study, and eligibility status
- Manage large data sets produced by external contracted sources and fit to study needs
- Conduct protocol specific patient visits
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Research Nurse Coord Resume Examples & Samples
- Serves as site Study Coordinator; maintains essential study documents for the sickle cell-hematology study protocols
- Conducts informed consent process as designated by principal investigator (PI) for the neurocognitive study that includes brain MRI and psychometrics on sickle cell patients
- Assists PI with sickle-cell-hematology study protocol submissions (internally sponsored and/or externally sponsored) for review by federal or institutional committees (e.g. CPSRMC and IRB) as applicable
- Collaborates with other clinical staff and performs routine tests as specified in assigned protocol(s) (e.g., temperature, blood and urine tests, PK levels, etc.)
- Assists with technical, clinical procedures on patients including intake vitals, triage and discharges
- Identifies and assesses education needs of the patient and family. Instructs, monitors, and documents the correct use of medications. Coordinates patient care with local physician or designee. Discusses pain management
- Documents patient education in chart. Assesses medical/psychosocial needs. Arranges clinic visits and ensures compliance with sickle cell disease, its treatments, complications and best preventative care
- Develops, maintains, and/or monitors case report forms from Sickle Cell-Hematology studies
- Provides data to the collaborating research organizations (CRO) or study/funding sponsors
- Performs data abstraction, collection, and entry to support clinical research on sickle cell patients
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Clin Research Nurse Coord Resume Examples & Samples
- 1 year of clinical research experience
- 1+ years of clinical research experience in a hospital setting or Pediatric clinical research experience preferred
- Experience working with Study Manager clinical trial management software, desired
- Graduation from an accredited school of Registered Nursing; Bachelor of Science degree in Nursing (BSN)
- Appropriate knowledge of anatomy, physiology, disease process and standard treatment protocols
- Experienced with inpatient and outpatient protocols
- Knowledge of Good Clinical Practice and ICH guidelines as adopted by the FDA
- Working knowledge of hospital research policies and procedures, IRB's, and FDA regulatory requirements for clinical studies
- Ability to think critically,take direction and establish priorities for the accomplishment of work assigned
- Skilled at chart review and abstracting data from patient charts
- Competent in MS-Word and MS-Excel applications
- Possesses interpersonal skills necessary to work effectively with patients, nursing and ancillary staff in a variety of contact settings
- Strong oral and written communication skills required for patient education, study subject enrollment, multi-disciplinary appointment coordination, and active participation in study team meetings
- Ability to work independently and to collaborate with team members as necessary
- Pediatric Advanced Life Support (PALS),Cert Phlebotomist Tech 1 CCRC or CCRP certification, preferred
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Travel Research Nurse Resume Examples & Samples
- Travel to different out of town locations to assist with the collection of data for clinical research protocol subject visits; This may include obtaining medical history and/or questionnaires, administering allergy skin tests, blood drawing, pulmonary function tests, assessing blood pressure and pulse, and instructing in and demonstrating the use of equipment and/or procedures to be used by participants
- Maintain accurate and detailed records in accordance with Federal Regulations as well as study protocols; This includes administration of and maintenance of consent documents, questionnaires, screening of medical tests for abnormalities, regulatory binder documents, sponsor and other regulatory binder documents. Responsible for taking appropriate actions to inform subject’s and/or investigators when appropriate
- Assess eligibility for recruitment by contacting, scheduling, and screening potential participants using various questionnaires and/or medical tests; This requires intense persistence in maintaining contact with participants, and may require occasional evening or weekend hours
- Direct experience in Human Subjects Research
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Research Nurse Resume Examples & Samples
- Basic computer proficiency inclusive of ability to access, enters, and interpret computerized data/information
- Effective interpersonal skills to facilitate communication with various members of the health care team, patients, and families
- Ability to effectively delegate appropriate patient care activities
- Ability to effectively manage stress due to critical issues related to patient care, changing organizational climate and personnel issues
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Research Nurse Resume Examples & Samples
- Provide advanced expertise in clinical study coordination and implementation, data and protocol management
- Oversee the coordination, tracking, data abstraction and collection, data reporting; pro-vide assistance with special procedures and clinical studies focused on lysosomal disorders and neurodegenerative disorders in affiliation with an institute or Clinical Center program of research
- Serve as an Associate Investigator on clinical protocols
- Ensure that all aspects of Good Clinical Practice GCP and federal regulatory requirements are met or exceeded and comply with all mandatory NIH training requirements
- Coordinate the recruitment, scheduling and intake of patients; manage challenging patient or protocol populations; complete intake tools, screening forms and general administration of protocol s implementation
- Collaborate with other disciplines in obtaining and maintaining informed consent/assent and addressing complex ethical and legal implications of same
- Perform data management through Labmatrix, CIT, CRIS and SharePoint; monitor to ensure accurate and reliable data entry; ensure pristine record keeping of all enrolled patients and families as is standard practice; ensure that security assurance of sensitive patient da-ta is of utmost importance, with all data in strict compliance with NIH policies
- Interact with patients of different ages, including pediatric and geriatric patients
- Identify which patients are due for follow-up evaluations; track study participants
- Screen inquiries from prospective patients
- Coordinate weekly clinical research meetings with clinical staff
- Act as point of contact among lab personnel, families and phlebotomy services to ensure timely acquisition and receipt of samples
- Report data to appropriate regulatory and monitoring agencies; anticipate and create database/data capture forms to meet protocol needs; share data collaboratively
- Pursue activities to facilitate the ease of reporting, avoidance of repetition of data entry procedures and generation of reports appropriate to various agencies. Serve as an expert consultant in matters related to the research process and specific, com-plex patient populations; consult and collaborate with medical and multidisciplinary staff colleagues from the specific institute, department or program; specialize in patients with Gaucher disease and /or Parkinsonism
- Provide on-call services to the multidisciplinary team, relevant to all matters of clinical re-search issues, specifically for patients with lysosomal or movement disorders, who are seen on-site
- Provide mentorship to staff nurses, developing skills and expertise in particular program areas; provide in-services to inpatient and outpatient unit nursing staff, as well as informal education to care providers in-house, in order to ensure complete and competent care for these patients
- Serve as a consultant and role model for professional practice, collaboration and communication
- Participate in clinical practice and research support meetings and develop multidisciplinary performance improvement programs and projects
- Collaborate with peers and other multidisciplinary team members to analyze and evaluate current systems of health care delivery and to identify and implement new practice patterns as appropriate
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Research Nurse Resume Examples & Samples
- Provide clinical care and direct nursing support for the Dermatology Branch outpatient research programs
- Document patient care via established guidelines
- Assess, plan and follow up with disease noted attributes
- Coordinate various activities (research subject schedules, data and biospecimen collection, and nursing care) to ensure proper and timely filing of standard clinical/regulatory documentation, serious adverse events, amendments, annual reports and other regulatory documents
- Recruit and enroll research subjects
- Develop patient rapport and work with staff on explaining protocol and tests/procedures to the patients
- Consult with health care professionals regarding medical, psychological and/or social patient needs
- Work with medical staff on skilled procedures
- Order protocol-mandated tests, labs and procedures
- Distribute biodspecimen kits; coordinate biospecimens for testing and diagnostic and research purposes (including referring MDs, NIH labs and repositories) and log biospecimen samples in appropriate database
- Follow subjects between visits; collaborate with community physicians to further the continuity of care and protect the integrity of the clinical research protocol/data
- Serve as liaison between clinical and laboratory sites, and with Principal Investigators (PIs)
- Work with staff on clinical research protocol development
- Work with staff to develop procedure manuals for clinical research protocols
- Work with staff to create case report forms
- Visit off-site collaborative centers
- Oversee ongoing protocol operations to ensure study compliance; troubleshoot possible protocol violations
- Work with staff on maintaining current regulatory documentation form numerous ongoing clinical research protocols
- Interface with NIAMS/NIDDK or other relevant Institutional Review Board (IRB); coordinate filing of Ups, AEs, amendments, continuing review applications, annual reports, protocol inactivation and other regulatory documents
- Work with staff on the management of research subject files; copy and organize research data
- Work on updates for clinical staff on patient care, protocol process and progress, human rights protection, ICH Good Clinical Practices and quality assurance education
- Collaborate with PIs to interpret research data for protocol team
- Work with investigators and medical writers on the production/revision of clinical research protocols
- Support the needs of data integrity and retrieval
- Participate in quality improvement and quality assurance initiatives involving database and data system development efforts
- Work with staff to identify the responsible party for data input into ClinicalTrials.gov at study conclusion, as applicable
- Participate in efforts to ensure scientific quality and human subjects’ protection
- Interact with auditing and monitoring agencies to facilitate the exchange of data
- Interface with other protocol support personnel
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Research Nurse Clinician Resume Examples & Samples
- Graduate of an accredited school of nursing, with a license to practice in the State of New Jersey
- One (1) year of oncology experience, is required
- Oncology Nursing Society (ONS), certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN), is preferred
- Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP), is preferred
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Network Float Research Nurse Resume Examples & Samples
- Collaborates with Care Coordination for all patient care referrals
- Collaborates with primary nurse in assuring that patient care needs are met
- Provides protocol education to patients and families; adapts interactions based on age-specific needs of the patient
- Collects and prepares required specimens for analysis and monitors test results, as appropriate
- Documents in charts as appropriate and communicates observations and findings to protocol investigator and attending physicians
- Provides protocol in-service training and serves as a resource to the health care team
- Maintains clinical practice that is evidence-based and consistent with nursing policies, procedures, licensure/registration requirements, and professional scope and standards
- Participates in QA/QI projects for the clinical program and the Division of Nursing and Patient Care Services
- Administers medications as necessary
- Maintains BLS certification
- Adapts to site specific policies, procedures and processes, communicates variations to Director of Research
- Quickly builds relationships with patients across multiple settings, supports the role of the primary nurse
- Demonstrates understanding of special needs and behaviors of age groups of the population served: all age groups, infants to geriatric
- Demonstrated flexibility and ability to work as an effective member of an interdisciplinary team
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Research Nurse Resume Examples & Samples
- Assumes responsibility for the effective operation of research protocols in collaboration with the principal investigator and study sponsor
- Assesses patients for protocol eligibility through personal interviews and medical record review in the outpatient and inpatient and settings
- Accurate and successful patient recruitment, scheduling and retention
- Coordinates and monitors patient associated with a protocol
- Collaborates with the multidisciplinary team as necessary
- Provides documentation in the patient’s medical record or recruitment log per protocol and institutional requirements
- Responsible for designated secondary protocol assignments
- Accurately reviews new protocol assignments for consistency and clarity
- Creates detailed data collection source document tools and routine protocol orders
- Responsible for day to day regulatory management
- Assists the primary investigator in collection and evaluation of data
- Retrieves protocol-related data as documented in the medical record and accurately enters it into computerized database
- Evaluates response to treatment, treatment toxicities and adverse drug reactions and reports appropriately to the principal investigator, the Institutional Review Board and the study sponsor
- Provides protocol summary reports as requested
- Assists the PI and support staff with protocol management, content and data analysis
- Participates in organization/coordination of information expected to be monitored/audited
- Participates in protocol-specific tasks as needed
- Identifies and provides patient and family education needs regarding treatment management, evaluation and follow-up in clinical trial through talking with patients person-to-person or by telephone and/or through written educational material
- Prepares for external monitoring or auditing visits
- Administers investigational medications as required by the protocol, following acceptable nursing procedures/guidelines
- Orders protocol related tests, procedures and consults
- Participates in budgets and research related charges for assigned protocols
- Maintains a high level of professional expertise and credibility through educational programs
- Keep current concerning research, oncology and data management issues through reading, attending meetings and inservices
- Attends departmental research meetings and conferences
- Attends approved off-site meetings, workshops and conferences
- Participates in National organizations that are oncology and research focused
- Provides professional and ancillary staff education concerning research protocols by presenting inservices in clinic and inpatient units
- Provides accurate information as requested to the multidisciplinary team
- Maintains appropriate license and certification
- Completes all mandatory institutional training requirements
- Successfully completes RNDM level 1 within six months of hire & RNDM level 2 within 2.5 years of hire
- Other Functions
- Retrieve and visually reads patient’s medical record
- Have a good command of the English language and be able to communicate well verbally and in writing
- Must be able to understand verbal and written directions
- Manually operates a personal computer via a keyboard
- Conduct personal interviews with patients in clinic or in-patient rooms or by talking on the telephone and contact local physicians by telephone or letter when necessary for protocol follow-up
