Research RN Resume Samples

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BB
B Brekke
Brandy
Brekke
709 Nikki Junction
Dallas
TX
+1 (555) 779 2129
709 Nikki Junction
Dallas
TX
Phone
p +1 (555) 779 2129
Experience Experience
Boston, MA
Research RN
Boston, MA
Ernser, Kemmer and Kub
Boston, MA
Research RN
  • Assist in recruiting existing subjects for future trials to ensure study timelines are met
  • Maintain current awareness and knowledge of research protocols; attend education sessions provided to research staff on trial conduction or research projects
  • Works collaboratively with other members of the client and patient care teams to ensure optimal outcomes and care
  • Performance-based rewards based on stellar individual and team contributions
  • Enjoys working with a diverse group of clients and patients, and scientists and clinicians within and outside of HLI
  • Other duties and responsibilities as assigned including but not limited to
  • Award-winning education and training across multiple career paths to help you reach your potential
Detroit, MI
RN, Clinical Research
Detroit, MI
Schiller-Casper
Detroit, MI
RN, Clinical Research
  • 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
  • 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
  • Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors
  • Knowledge of medical terminology, nursing assessment, clinical trials and GCP concepts
  • Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities
  • Current licensure as a registered nurse in state of practice
  • May collaborate with Research Site Leader in the study selection process
present
Boston, MA
RN Research Coordinator
Boston, MA
Fritsch-Weber
present
Boston, MA
RN Research Coordinator
present
  • Provides consultation and/or assistance to units and/or clinics as it relates to study patients, protocol and research guidelines
  • Educational programs for patients, staff and faculty are developed and delivered
  • Assists the Principal Investigators during audits by sponsoring agency or other regulatory bodies
  • Be responsible for assisting the Investigator in accomplishing successful research trials
  • Assists with the recruitment, selection, scheduling, and monitoring of research project participants. Manages the handling of adverse events, compliance and other participant-related issues
  • Performs surveillance of research patient units for monitoring of results and detection of adverse events as a result of study protocol
  • Work to screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring of the subjects participating in the research study
Education Education
Bachelor’s Degree in Nursing
Bachelor’s Degree in Nursing
Boston University
Bachelor’s Degree in Nursing
Skills Skills
  • 9) Demonstrates competency in performing training, education, fiscal responsibilities, associated administrative processes, professional interactions with staff and others
  • 3) Supports and enhances patient centered care using a knowledge of disease processes and patients ' values and goals
  • 4) Acquires knowledge and skills (e.g., motivational interviewing) to maintain expertise in area of practice
  • 6) Evaluates practice of self and others using professional standards, relevant statutes, and regulations, and takes action to improve performance
  • 5) Provides structured nursing assessment and/or intervention over the phone or in person
  • 7) Recognizes emergency situations and responds appropriately
  • 8) Uses a body of research to validate and/or change work group practice
  • 2) Conducts or evaluates research interventions
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15 Research RN resume templates

1

Research Rn-otolaryngology Resume Examples & Samples

  • Common ENT conditions
  • Institutional Review Board (IRB) paperwork and procedures
  • Clinical Trials Management System (preferrably Velos)
  • Ability to multitask, be organized and handle multiple clinical trials
  • Professional
  • Adaptable to change
2

Oncology Research RN Specialist Resume Examples & Samples

  • Prepares and submits information from patient�s chart and other source documents on appropriate data forms/flowsheets/databases
  • Maintains supply inventory with critical focus on expiry management
  • Assists with the coordination of research monitor visits and audits; prepares appropriate data
  • Assists in the collection, preparation and shipping of samples
  • Supports the clinical trial team to efficiently complete tasks including documentation/submissions, Serious Adverse Events (SAEs)/safety reports, FDA Form 1572, DARFs, ClinicalTrials.gov postings, etc
3

Oncology Research RN Spec-levine Cancer Institute Resume Examples & Samples

  • Assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within LCI
  • Maintains protocol amendments, deviations, and informed consent changes regarding oncology research studies, assuring all documentation is managed compliantly and maintained in an audit-ready manner
  • Assists in the monitoring of clinical trial compliance by reporting issues and problems appropriately
  • Obtains required documentation (forms, slides, reports, etc.) to assess patient eligibility for research studies
  • Obtains and completes data for patients enrolled on clinical trial
  • Completes/resolves queries from sponsors
  • Obtains required forms, slides, reports, and other information needed to assess patient eligibility
  • Maintains patient shadow charts with appropriate source documentation
  • Completes registration for patient enrollment and maintains status in sponsor and LCI databases
  • Assists in writing/updating Informed Consents with PI and team
4

Rn-oncology Specialist Research Days CHI Health Good Samaritan Resume Examples & Samples

  • Requires a minimum of two years of oncology experience
  • Previous experience preferred in coordinating activities associated with clinical trials: including recruitment, eligibility screening, medical management, education and training of staff and patients, administration, data management and compliance
  • Demonstrated knowledge and competency in chemotherapy
  • Demonstrated knowledge of symptom management principles for persons undergoing chemotherapy, radiation therapy and biotherapy
  • Competent PC-based computer skills (except where more advanced skills indicated) in basic software programs. Knows how to analyze and manipulate data in spreadsheets and control charts
  • Knowledge and application of age-specific care and teaching
  • Knowledge and application of research utilization as a basis for clinical decisions and practice
  • Knowledge of adult-learning principles
5

Rn-research Coordinator Resume Examples & Samples

  • Exhibits thorough knowledge of database application programs
  • Assists, updates and communicates with members of the disease portfolio team by providing knowledge of assigned protocols. Ensures timely and accurate reporting of all Adverse Events
  • Enters patient information into clinical research database and maintains patient information in research database to ensure proper research accounting
  • Assists with the training of new staff as needed
  • Performs internal quality assurance audits of research records as requested by managers or outlined in the research quality management plan
  • Identifies problems or obstacles in the system/procedures related to implementation of the research protocols. Communicates with study investigators and works collaboratively for resolution
  • Authorized to make entries in the medical record, consistent with and limited to the scope of job duties and applicable licensure
6

Research RN 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
  • Consistent, regular, punctual attendance as scheduled is an essential responsibility of this position
  • Dedication, above all, to caring for patients suffering from chronic kidney failure across the nation
  • 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
  • Current CPR certification required
  • Basic computer skills and proficiency in MS Word Outlook required
7

Oncology Research Coordinator RN Resume Examples & Samples

  • 2 years as a research data coordinator or position requiring preparation and conduct of research studies
  • Knowledge and understanding of oncology and disease processes as applied to clinical research
  • Demonstrates good leadership, decision-making and judgment skills. Analytical skills to evaluate information, practices and procedures, formulate logical and objective
  • Conclusions and make recommendations for effective solutions
  • Good organization, communication and planning skills
  • Knowledge of basic anatomy and medical terminology
  • Ability to work closely with caregivers and with patients who have a terminal illness
  • Good writing skills including ability to compose reports and correspondence while utilizing correct grammar, spelling and punctuation as well as clearly documenting research data onto forms
  • Possess mathematical abilities to perform calculations involving basic accounting, body surface area (BSA) calculation and drug dosage calculations
  • Ability to meet the scope of the program with general supervision and with frequent changes in priorities and deadlines
  • Working knowledge of Microsoft Word and Excel. Ability to work cooperatively as a team member in a diverse workforce
  • Must be able to write effectively for a variety of audiences, both professional and lay
8

Oncology Research RN Spec Resume Examples & Samples

  • Participates in the study project start-up activity, working with the PI and others to initiate new research projects
  • Maintains appropriate documentation, (i.e. FDA Form 1572, CTSU documentation, IRB approval letters, ICFs, etc.) for assigned studies
  • Assists in maintenance of filing systems, data repositories and systems
  • Contacts local research staff to confirm scheduling of tests/treatments required by protocol
  • Completes Case Report Forms (CRFs) maintaining high level of accuracy
  • Assists with inventory, ordering, organization and distribution of supplies related to assigned trials
  • Maintains regulatory binder for review at monitoring visits
  • Assists with the coordination of required protocol-related activities such as tests and treatments using CTMS
9

RN Cancer Research Coordinator Resume Examples & Samples

  • Registered Nurse with California license
  • Master's Degree in Nursing with concentration in a cancer clinical area
  • 3 to 5 years nursing experience in acute hospital clinical service areas
  • Prefer 2 or more years experience with assessing and enrolling patients onto clinical trials
  • Knowledge of research methods and design are strongly preferred
  • May be required to visit multiple worksites across the peninsula area (inpatient, physician practice, outpatient facility, etc)
10

Research Rn-oncology Services Resume Examples & Samples

  • High level of physical assessment skills needed in order to complete study protocols and manage patient
  • Basic computer skills required in order to input patient data into national web based Data Base
  • Ability to be flexible regarding scheduled work hours in order to enroll participants when they become available for research studies is desirable
  • Excellent customer service orientation skills necessary in order to deal effectively with various levels of hospital personnel, outside customers and community groups
  • Three years working experience as an RN with emphasis on patient physical assessment in order to complete research study protocols and manage patient care
  • Knowledge of managing clinical research protocol and research oriented data collection process
  • Knowledge of FDA Regulations and GCP guidelines
  • In collaboration with the investigator(s) and other team members, manages a case load of research patients including
11

Rn-research Coordinator Resume Examples & Samples

  • Registered Nurse licensed in the State of Michigan
  • BSN preferred
  • Must have a minimum of three years of nursing experience
  • One year of clinical research experience preferred
12

Research RN Resume Examples & Samples

  • 1) Applies the nursing process to systems or processes for planning, organizing, directing, and evaluating patients care needs
  • 2) Conducts or evaluates research interventions
  • 3) Supports and enhances patient centered care using a knowledge of disease processes and patients ' values and goals
  • 4) Acquires knowledge and skills (e.g., motivational interviewing) to maintain expertise in area of practice
  • 5) Provides structured nursing assessment and/or intervention over the phone or in person
  • 6) Evaluates practice of self and others using professional standards, relevant statutes, and regulations, and takes action to improve performance
  • 7) Recognizes emergency situations and responds appropriately
  • 8) Uses a body of research to validate and/or change work group practice
  • 9) Demonstrates competency in performing training, education, fiscal responsibilities, associated administrative processes, professional interactions with staff and others
  • Occasional travel throughout the Denver metro area
  • Nurse I Level I - An Associate Degree (ADN) or Diploma in Nursing, with no additional nursing practice/experience required
  • Nurse I Level II - An ADN or Diploma in Nursing and approximately 1 year of nursing practice/experience; OR an ADN or Diploma in Nursing and a bachelor's degree in a related field with no additional nursing practice/experience; OR a Bachelor's of Science in Nursing (BSN) with no additional nursing practice/experience
  • Nurse I Level III - An ADN or Diploma in Nursing and approximately 2-3 years of nursing practice/experience; OR an ADN or Diploma in Nursing and a Bachelor's degree in a related field and approximately 1-2 years of nursing practice/experience; OR a BSN with approximately 1-2 years of nursing practice/experience; ORa Master's degree in nursing (MSN) or related field with a BSN and no additional nursing practice/experience
  • Nurse II - A BSN with approximately 2-3 years of nursing practice/experience; OR ADN or Diploma in Nursing and a Bachelor's degree in a related field and approximately 2-3 year's of nursing practice/experience; OR a Master's degree in nursing or related field with a BSN and approximately 1-2 year's of nursing practice/experience; ORa Doctoral degree in nursing or meets basic requirements for appointment and has doctoral degree in a related field with no additional nursing practice/experience required
  • Nurse III - Master's degree in nursing or related field with BSN and approximately 2-3 year's of nursing practice/experience; OR a Doctoral degree in nursing or related field and approximately 2-3 year's of nursing practice/experience
  • Outpatient care, ideally of patients with heart failure or COPD
  • Motivational interviewing
  • Palliative care
  • Current Basic Life Support (BLS) certification for a healthcare employee by an approved provider
  • Current Advanced Life Support (ACLS) certification for a healthcare employee by an approved provider
  • Heavy Lifting, 45 pounds and over
  • Heavy Carrying 54 pounds and over
  • Straight pulling (2-6 hours)
  • Pushing (2-6 hours)
  • Reaching above shoulder
  • Use of fingers
  • Both hands required
  • Walking (5-9 hours)
  • Standing (4-8 hours)
  • Kneeling (1-2 hours
  • Repeated bending (2-4 hours)
  • Climbing, legs only (1-2 hours)
  • Twisting (2-4 hours)
13

RN Clinicial Research Specialist Resume Examples & Samples

  • Ensures that the clinical research staff and/or students conduct the clinical aspects of the projects appropriately and adhere to the clinical trial schedule, which may include: maintaining, dispensing and recording drug and medical device supplies according to regulations; assisting in obtaining informed consent from project participants; assisting in the development and implementation of case report forms; instructing volunteers on protocol requirements and explaining procedures and consent forms; performing research patient registration; ensuring that clinical research staff conduct the clinical aspects of the projects appropriately and adhere to the schedule of the clinical trials; serving as an advocate for the research participant, assisting them through the research process; and/or, performing other related activities
  • Develops and maintains regulatory and legal documents per guidelines and regulations of the research/study sponsor and the participating institution per IRB, FDA, PHA and other applicable regulatory agencies. Assists in annual reporting to Federal agencies as required
  • Assists in the development and maintenance of budget and/or contract agreements. Follows policy requirements for reporting patient enrollment in an effort to ensure compliance with billing. Assists in the development of accounting reports and in coordination of billing systems
  • Coordinates and safely implements research activities through interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board (IRB)
14

Rn-research Coordinator Resume Examples & Samples

  • Identifies and recruits patients into study protocols as needed
  • Provides for educational and/or emotional support to patients enrolled in the study protocol
  • Is responsible for managing the study documentation and data collection for the study, and preparing and monitoring the budgets as needed
  • Supports physician investigators and other clinicians as necessary to facilitate project participation and compliance
15

RN Clinical Research Supervisor Resume Examples & Samples

  • Supervises the clinical research operation in a practice for all research staff members in accordance with USON SOP and ICH GCP guidelines. Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice
  • Collaborates with the SRL, physicians of the practice and research committee in the process of study selection for the research program. Develops and implements research budgets that include accrual targets and financial objectives for each research location, in collaboration with practice management. May promote or market research program to the practice, community and referring physicians. May coordinate research activities with other (non-USOR) bases or sponsors
  • Develops research accountability standards, metrics, and reports and identifies areas for improvement. Collaborates with site research leader (SRL) and research staff in the implementation of action plans designed to improve practice research operations and quality assurance functions
  • Implements short term goals that align with the companys vision and business goals. Cascades goals down to staffs annual objectives
  • Provides on-going job related education and training to staff. May develop training materials. Develops and maintains standard operating procedures (SOPs) continually improving efficiencies
  • Coaches and develops staff. Responsible for recruitment, interviewing, recommending hires, assessing performance, recommending salary changes, and progressive discipline. Enforces adherence to Company policies
16

Rn-research Resume Examples & Samples

  • Organizes research protocol to include, but not limited to, obtaining consents
  • Assists in preparation of information for submission to Institutional Review Board (IRB) for approval and completes correspondence between IRB and drug companies
  • Serves as Iowa Heart Center’s resource and liaison in all aspects of each protocol to study with patients, families, hospitals, office staff, physicians, pharmaceutical companies and coworkers
  • Completes all necessary paperwork connected to research study
  • Coordinates all activities related to patients’ diagnostic testing, visits and evaluations
  • Organizes and assists with site visits with drug companies and monitors CRA
  • Organizes and participates in meetings as required for orientation to study, update or review, etc
  • Provides backup and maintains an understanding of all other protocols which the group is involved in for support and relief of primary nurse on projects
  • Conducts in-service education where needed
  • Conducts patient phone calls or follow-up assessments as needed
  • Participates in professional development activities and maintains professional affiliation and certification
  • Maintains statistical collection of all protocols
  • Administration of research protocols by finding patients who meet inclusion/exclusion criteria, scheduling in office doctor and lab visits. Coordinate and/or perform other tests in and outside the clinic. Maintain accurate documents, FDA records and case form records, complete health and drug histories and disease assessments. Review patient data for safety and administration purposes. Make corrections and clarifications of data for sponsor monitors
  • Assess learning needs of patient and significant others. Teach patients about medications and procedures of protocol. Gives accurate and complete information Obtains patient consent signatures after instruction completed
  • Writes patient consent forms to meet HIPAA, FDA, INH and IRB requirements
  • Follow guidelines for human subjects
  • Travels to Iowa Heart offices as needed
  • Certified in handling, packing, and transportation of hazardous materials, (ie.blood)
  • Performs other related work as required
  • Current licensure as R.N., state of Iowa or compact state
  • Valid Iowa Driver’s/Chauffeurs License required, must meet Mercy’s Motor Vehicle Safety Standards, must be at least 18 years of age and be eligible to drive per Iowa state law
  • Three years of RN nursing experience required. Two years of critical care experience preferred or clinical cardiac equivalent experience required
  • Proof of completion of Mandatory Reporter abuse training specific to population served within three (3) months of hire
  • Basic Life Support (BLS) for the Healthcare Provider certified or obtained by the end of the orientation period (approximately six (6) weeks)
  • Level I Cardiac Arrhythmia class completion within 6 months of hire
  • Demonstrates a commitment to service, organization values and professionalism through appropriate conduct and demeanor at all times
17

Rn-clinical Research Hope-nw / Tucson Resume Examples & Samples

  • Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research
  • Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality
  • 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
  • Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials and GCP concepts
  • Ability to work independently, organize, prioritize, and follow through with results
18

RN Research Coordinator Resume Examples & Samples

  • Coordinates the preparation and delivery of departmental communications, presentations and marketing/educational materials
  • Contribute to Mission effectiveness by promoting the spirit embodied with the Mission Statement: A. Service to the poor - Support the cause of those who lack resources for a reasonable quality of life.B. Reverence - Respect and compassion for the dignity and diversity of life.C. Integrity - Inspiring trust through personal leadership.D. Wisdom - Integrating excellence and stewardship.E. Creativity - Courageous Innovation.F. Dedication - Affirming hope and joy in our ministry
  • Collects research data, submits reports data and reports as requested or required by study sponsor IRB, or others. All other duties as assigned
  • Screens and recruits participants for research trials according to protocol clinical criteria and federal regulations. Obtains informed consent in accordance with Good Clinical Practice and federal regulations
  • At least three (3) years research or recent hospital experience
19

Research RN Resume Examples & Samples

  • BSN from an accredited program for nursing
  • Required: Current and unrestricted Registered Nurse license in the state of Rhode Island
  • Required: At least 5 years of nursing experience
  • Preferred: At least 5 years of direct experience with IV insertion, phlebotomy, and related procedures. Must demonstrate competence in IV/phlebotomy checklist by end of introductory period or position will be forfeited
  • Preferred: At least 5 years of experience with blood sample processing strongly preferred
  • Preferred: At least 5 years of related work experience in clinical/laboratory research setting preferred
  • Preferred: Experience in administering EKGs preferred but not required
  • Strong communication skills and ability to work as part of a team
  • Flexibility, accountability, and responsibility
  • Ability to work independently, prioritize tasks efficiently, take initiative, and maintain highly organized working conditions
  • Knowledge of aseptic technique and Universal Precautions
  • Ability to calculate figures and amounts such as proportions, percentages, and volume
  • Understanding of experimental research methodology and clinical research procedures
  • Experience and proficiency with computer applications, including internet, word processing, and data management applications
20

Rn-cardiac Research & Registries Coordinator Resume Examples & Samples

  • Computer skills in data base management, word processing, graphs and presentation
  • Excellent communication and teamwork skills
  • Ability to use other office equipment as necessary to accomplish daily work
  • Must have excellent interpersonal skills to interact with patients and physicians
  • Database data entry and/or management experience preferred
  • Quality improvement or patient safety knowledge and experience preferred
  • Assists in study budget management, IRB submissions and new study requirements
  • Review Eligibility and register only patients who meet eligibility requirements onto studies
  • Meet with potential research patients to explain studies and assist the physician in the consent process
  • Complete basic eligibility review and provide requested information to physicians within 24 hours of request
  • Coordinate the research patient’s care including developing an individualized patient orders calendar for each patient and each study
21

RN Research Resume Examples & Samples

  • Two years of nursing experience necessary
  • The job incumbent is required to demonstrate the knowledge and skills necessary to provide patient care appropriate to the age and disease of the patients served
  • This requires that the incumbent demonstrates knowledge of the principles of growth and development as well as the physical, emotional and psycho-social needs of the patient population served
  • Current State license as a Registered Nurse required
  • Professional knowledge of nursing theory and practice at a level normally acquired through completion of two years training at an accredited School of Nursing in order to be eligible for licensure as a Registered Nurse
  • Interpersonal skills necessary in order to interact with patients, families, physicians, and to demonstrate sensitivity necessary to elicit patients’ cooperation and allay anxiety
  • Analytical skills necessary in order to gather and interpret data relevant to research and neurological complications
22

Research RN Resume Examples & Samples

  • Associates of Science Degree in Nursing (ASN) from an accredited school of nursing
  • Current California RN license
  • Three to five (3-5) years RN work experience in an ambulatory care setting or sub-specialty
  • Current BLS for Healthcare Providers certificate by start date
  • Knowledge of basic triage skills
  • Must have an interest in research, with critical attention to detail
  • Maintains safe and clean working environment by complying with procedures, rules, and regulations
  • Proficient with MS Office
  • Excellent communication and customer service oriented
  • Collaborate with colleagues to assist patients in their care and testing
  • Identifies patient service requirements by establishing personal rapport with patients and customers
  • Self-directed
  • Ability to work well with teams in an open environment
  • Demonstrate sound judgment to effectively solve problems and think critically
  • Maintains patient confidentiality and protects operations by keeping patient care information confidential and following HIPAA practices
  • Bachelors of Science Degree in Nursing (BSN)
  • Experience with clinical research protocols
  • Knowledge and experience with respiratory care and pulmonary function testing
  • Customer focused to provide a high level of care and a positive experience
  • Dynamic individual with the ability to communicate and engage others
  • Interest in Cardiology and experience performing exercise stress tests
  • Open to learning new things for cross-training potential
  • Interest in taking on new challenges
23

Rn-research Resume Examples & Samples

  • Screens all potential and physician-referred patients for protocol eligibility. Maintains and submits monthly screening logs
  • Presents trial concepts and details to the patients, and participates in the informed consent process under the direction of the physician
  • Documents informed consent process and all components of protocol treatment. Participates in ongoing patient education. Coordinates scheduling of tests and treatments required for the protocol. Maintains research patient database according to US Oncology Research (USOR) Standard Operating Procedure (SOP)
  • Assesses patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug, and thoroughly documents all findings
  • Works directly with the physician/investigator and clinic staff to ensure protocol compliance
  • Reports to practice operations and physicians regarding monthly accrual statistics and financial status. May be responsible for creating budgets for the research department. Coordinates payment of non-standard of care protocol-required procedures in order to be compliant with federal and state billing regulations
  • Ensures accurate and complete data collection, entry, and timely submission to central operations in accordance with USOR SOP
  • Coordinates research drug procurement and accountability records in accordance with USOR SOP
  • Participates in and supports all site auditing and monitoring visits
  • Maintains protocol regulatory documents in compliance with USOR SOP. Communicates, reviews, and documents weekly Regulatory Memoranda with physicians and other clinic staff as appropriate
  • Oversees local quality assurance program and develops appropriate action plans for quality improvement
  • Actively participates in protocol initiations and study specific educational programs. Communicates and collaborates on an ongoing basis with central operations
  • Graduate from an accredited RN program and bachelors in science or healthcare field is required (BSN preferred)
  • Three years of clinical research experience preferred
  • Current licensure as a registered nurse in state of Nevada
  • Current BLCS or ACLS certification required
  • Experience with computer data entry and database management
  • Ability to read, analyze and interpret technical procedures such as protocols, informed consent documents and regulatory documents
24

RN Research Coordinator Resume Examples & Samples

  • Performs surveillance of research patient units for monitoring of results and detection of adverse events as a result of study protocol
  • Provides consultation and/or assistance to units and/or clinics as it relates to study patients, protocol and research guidelines
  • Educational programs for patients, staff and faculty are developed and delivered
  • Assists the Principal Investigators during audits by sponsoring agency or other regulatory bodies
  • Tracks appropriate data to assess patient’s response to study protocol
  • Performs area-specific support/clinical activities
25

RN, Clinical Research 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
  • Graduate from an accredited program for nursing education (BSN preferred)
  • This is an entry level research nursing position requiring 1 year of experience, preferably in oncology
  • Current licensure as a registered nurse in state of practice
  • OCN, SoCRA or ACRP certification preferred
  • Knowledge of medical terminology, nursing assessment, clinical trials and GCP concepts
  • Ability to read, analyze, and interpret technical procedures such as protocols, informed consent documents, and regulatory documents