Research Coordinator Clinical Research Resume Samples

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EH
E Halvorson
Eldora
Halvorson
402 Jayden Springs
Dallas
TX
+1 (555) 446 1314
402 Jayden Springs
Dallas
TX
Phone
p +1 (555) 446 1314
Experience Experience
Boston, MA
Clinical Research Coordinator, RN
Boston, MA
Raynor-Fisher
Boston, MA
Clinical Research Coordinator, RN
  • Acts as liaison between principal investigators and sub-investigators on all regulatory issues and changes within the protocol
  • In collaboration with the principal investigator, reviews studies for feasibility and evaluates potential competition with other protocols prior to submitting study
  • Reviews study with principal investigator to a budget outlining standard of care and research costs. Finalizes budget draft with budget coordinator
  • Recruits and evaluates study patients, schedule appointments and interviews
  • Reviews medical records for potential study patients and ensures that medical records include documentation of all laboratory test results and procedures and progress of study patients, following guidelines set forth by the protocol sponsors
  • Assists investigator with consent process assuring study patients understand clinical trials and obtains written informed consent
  • Educates study patients concerning informed consent procedures, HIPAA authorization
Los Angeles, CA
Clinical Research Coordinator Hoag Inst for Research & Ed
Los Angeles, CA
Hahn-Funk
Los Angeles, CA
Clinical Research Coordinator Hoag Inst for Research & Ed
  • Assist the Principal Investigator (PI) in the conduct of the clinical study according to FDA and Sponsor regulations and guidelines and ensures the safety and welfare of the research participants
  • Drafts or reviews template Informed Consent Forms with Clinical Research Office per FDA, ICH, GCP guidelines and Hoag Policy language
  • Perform other duties as assigned
  • Schedule or assist in scheduling follow-up visits for enrolled subjects
  • Documents and reports Unanticipated Problems, Adverse Events and Serious Adverse Events according to Clinical Research Office policy, Sponsor, IRB, FDA, ICH and GCP guidelines and specific protocol, to the Investigator, Sponsor, Clinical Research Office administrative staff, and IRB
  • Complete the Case Report Forms for the study accurately and completely. Abstract data from hospital record and physician charts to complete CRFs
  • Accommodates changes in workload within the department and demonstrates flexibility in accepting work assignments. Performs assignments as directed by Supervisor
present
Philadelphia, PA
Oncology Clinical Research Coordinator Days CHI Health Cumc Bergan Mercy
Philadelphia, PA
Kuphal, Keeling and Pacocha
present
Philadelphia, PA
Oncology Clinical Research Coordinator Days CHI Health Cumc Bergan Mercy
present
  • Participates in all mandatory quality improvement, safety, security, and infection control program
  • Collects, manages and maintains patient and laboratory data for clinical research studies
  • Serves as subject matter expert for all phases of the research trials as assigned
  • Enters patient information into clinical research database and maintains patient information in research database to ensure proper research accounting
  • Analyzes and abstracts data from departmental and medical record charts to complete and submit case report forms
  • 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
Education Education
Bachelor’s Degree in Sciences
Bachelor’s Degree in Sciences
Oregon State University
Bachelor’s Degree in Sciences
Skills Skills
  • Partner with members of the Operations and Research teams to play an active role in ensuring the success of Company-led research studies
  • Lead the preparation of clinical protocols, amendments, informed consent forms, study guides, case report forms, and any other clinical research related documents
  • Monitor performance of investigational sites
  • Educate study sites in correct collection, processing and shipping of biospecimens to central repository
  • Act as the voice of the Company with study participants and other external partners
  • Interact with potential study participants, educating them about the study including the possible risks/benefits, procedural details and significance of the study; answers study related questions posed via e-mail or phone calls from potential participants and/or the general public
  • Data collection and data entry, including performing regular audits to ensure that the data collected is complete and accurate
  • Assist with the production of participant education material, research newsletters, development of web content and online project communication
  • Communicate progress and research findings with regular presentations
  • Handle various administrative activities generally associated with conducting research studies
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15 Research Coordinator Clinical Research resume templates

1

Clinical / Translational Research Coordinator Resume Examples & Samples

  • Knowledge and understanding of the Federal regulations and guidelines governing the protection of human subjects, e.g., FDA, OHRP, GCP/ICH , and HIPAA regulations
  • Proficiently prepares and processes new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and departmental policies and procedures and federal regulations
  • Understanding and capability to accurately and compliantly perform the procedures required of each study protocol, working collaboratively with study participants, other staff and departments, in safely and accurately performing study procedures such as assessing participant eligibility and recruitment, arranging necessary schedules and procedures, completing required participant registration in StarPanel, conducting interviews and laboratory and diagnostic studies, tracking medication usage, etc. Ability to identify and troubleshoot problems
  • Accurately and compliantly prepares and maintains documents required to be maintained internally and available for regulatory authorities and/or the sponsor prior to, during and after the conduct of a clinical/translational trial. Participates in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation and research procedures
  • Identifies and procures equipment and supplies needed to fulfill project requirements (locally and across multiple sites, if required)
  • Participates in the determination of eligible candidates for study participation, assuring participants fulfill eligibility requirements. Strives to ensure studies are completed in a timely manner through implementing effective screening and recruitment strategies and completing required documentation
  • Records data from source documentation and/or participant interaction onto case report forms (either paper or electronic) with awareness and attention to the requirements for accuracy, completeness and timeliness. Attends to query resolution in a timely manner. Assures research information is collected and stored in a manner that is compliant with regulations/policies and good clinical practice. Participates in site visits from sponsor, regulatory authorities and others to review research, source documentation, critical documents and research procedures
  • Knowledgeable of the safety reporting requirements of the study protocol, IRB, FDA and other regulatory bodies. In a timely fashion, monitors, detects and reports adverse events meeting requirements of regulatory bodies. Coordinates activities and gathers information from a variety of sources to achieve stated outcomes
  • Performs packaging and ships study specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with sponsor and shipping guidelines and regulations, maintaining appropriate documentation
  • With direction, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance, providing reports investigators, department administration and funding agencies
  • Demonstrates initiative for continuous learning, both self-directed and as evidenced by attendance of educational and professional development opportunities. Actively seeks new learning opportunities, seeing learning as part of work
  • Engages in a minimum of 10 hours of continuous, job-related educational activities annually or pursuing an advanced career-related academic education or certification
  • Participates in and maintains certifications, licensure and credentialing as required by Vanderbilt, the department and Sponsor
  • Participates in research related programs, such as the Clinical/translational Research Staff Council and its activities by submitting issues or suggesting solutions, and reviewing Council information, by attending meetings open to research staff and by sharing information with other research personnel
  • Furthers knowledge by completing more advanced job-related educations (such as Research Support Services Boot camp Follow-up). Actively seeks new learning opportunities, seeing learning as a part of work. Develops and achieves personal and professional goals
2

Clinical Trials Research Coordinator Resume Examples & Samples

  • ComplianceSupport & comply w/ the Principles of Responsibility (Kaiser Permanente Code of Conduct). W/ guidance from PI, assist w/ ensuring compliance w/ KPNC IRB Standard Operating Procedures (SOP) & document applications. Adhere to Guideline for Good Clinical Practice (GCP), federal, state, & local regulations, & KP policies & procedures. W/ supervision, assist w/ preparation for inspections, audits & monitoring visits
  • Assist w/ obtaining medical records & test results for all projects/participants. w/ supervision & certification, perform packaging & shipping of protocol specimens to the Sponsor lab in accordance w/ IATA/DOT regulations & Sponsor shipping guidelines. Direct issues requiring medical decision-making to the appropriate licensed staff member promptly
  • This job description is not all encompassing
3

Clinical Trial Research Coordinator Resume Examples & Samples

  • Study Implementation: Maintain the security & confidentiality of participants' paper or electronic data (e.g., case report forms kept in a secure, locked space). Assist w/ scheduling participants for study assessments/visits, required tests including visit-specific laboratory kits and/or paperwork preparation. Prepare packets for participants (e.g., instructions, phone numbers, calendars, diaries, etc.)
  • Under specific direction, assist w/ data entry of study activity onto a case report form (paper or electronic), & maintain a database program to track all study activity (i.e., study enrollment & consents). Assist in maintaining research charts & site regulatory files. Assist in ensuring that study-related, non-test article supplies are shipped & re-supplied according to protocol, including tracking expiration dates. Assist in obtaining protocol specific regulatory documents including MDs/RNs licenses & CVs
  • Report any potential protocol violations/deviations to the PI in a timely manner. Support the regulatory team in the maintenance & storage of critical documents required to be maintained & provided to the Sponsor during the conduct of the trial. W/ supervision, assist in study closure activities including preparation & collection of close-out documentation, & preparation of study files for distribution to longterm storage
  • Clinical trials experience preferred
  • Primary responsibilities are to provide data management in a timely manner for patients on cancer trials including facilitating patient entry into programs and managing and collecting data for submission to research centers. Will manage all screening, active treatment and follow up data form submissions, xrays, and pathology specimens for all protocols patients. Will assist in the oncologists’ in ordering/scheduling specific protocol tests/appointments as directed. Will require travel by own reliable transportation to different centers to assist in patient enrollment and adherence to all research requirements. Maintain IRB regulatory material at the local site level. Coordinate adverse event/serious adverse event submissions to the IRB and sponsors. Prepare and assist in any required audits. Assist the Director and Manager of the Program in other assigned projects. Willing to abide by Good Clinical Practice Guidelines and all FDA regulations. CPR-certified required
4

Clinical / Tran Research Coordinator Resume Examples & Samples

  • Approximately 60% of time will be spent administering, scoring & entering standardized tests for various studies in the lab
  • Assist in the recruitment and screening of 900 students in the Nashville area
  • Maintain participant files (scanning consents, teacher paperwork, REDCap uploading of docs, move-to-server, etc.)
  • Assist in preparation of training materials for grants
  • Assist in auditing graduate research assistants’ test administration and scoring as needed
  • Assist in the preparation of materials for publication
  • Assist in general lab procedures as needed
  • Assist in planning for high-volume participant seasons, including preparation of materials, logistical planning, scheduling, & other duties as needed
  • Provide support as needed during high-volume participant seasons
5

Clinical Trials Research Coordinator Resume Examples & Samples

  • Study Implementation Maintain the security & confidentiality of participants' paper or electronic data (e.g., case report forms kept in a secure, locked space). Direct issues requiring medical decision-making to the appropriate licensed staff member promptly. According to protocol &/or IRB-approved telephone script, collect & document research data & report the information to the appropriate licensed staff member & PI for assessment in a timely manner. Coordinate & schedule participants for study assessments/visits, required tests, including visit specific lab kits &/or paperwork preparation, etc. Prepare packets for participants (e.g., instructions, phone numbers, calendars, diaries, etc.). W/appropriate guidance, obtain & review medical records & test results of all project/study participants & abstract needed data per protocol requirements. W/guidance from PI, complete case report forms (paper or electronic) & maintain a database program to track all study activity including study enrollment & consents. Respond to Sponsor to resolve data queries & delinquencies in a timely manner. Report any potential protocol violations/deviations to the PI in a timely manner. Assist in the collection of protocol required data w/ timely & accurate submissions as required by Sponsor (e.g., weekly screening log, routine electronic data submissions). Coordinate & prepare protocol specimens for shipping or storage in accordance w/ IATA/DOT regulations & Sponsor shipping guidelines. Assist w/ participant's long-term follow-up data collection. Assist PI &/or Clinical Trial Nurse, if applicable, w/ identifying, screening, & recruiting potential participants. Provide PI &/or Clinical Trial Nurse w/ the ongoing informed consent process by coordinating the current consent documents. Assist in study closure activities including preparation & collection of close-out documentation, & preparation of study files for distribution to longterm storage. W/guidance, receive, disseminate & maintain study-related communications w/ internal & external parties involved w/clinical trial protocols
  • One (1) year of experience in clinical trials research OR a bachelor's degree required
  • Current ACRP or SoCRA certification preferred
6

Research Coordinator Clinical Research Resume Examples & Samples

  • Bachelor Degree or equivalent experience
  • Patient care experience
  • Clinical Research experience
  • Regulatory guidelines regarding research (example: ICH-GCP and FDA regulations.)
  • Basic computer knowledge; must be able to perform cashier duties
  • Medical and nursing equipment and supplies
  • ECG machine
  • Oncology related experience
7

Clinical Research Coordinator Pulmonary Critical Care Resume Examples & Samples

  • Bachelor of Science or related degree
  • Master’s in Public Health or related clinical field
  • Experience in area of assigned clinical specialty
8

Clinical Trials Research Coordinator Resume Examples & Samples

  • Theoretical knowledge of a biological science such as Biology, Microbiology or a related field. Demonstrated knowledge of research methods
  • Demonstrated experience conducting clinical trials. Proven experience in research protocol start up procedures, marketing, outreach, recruitment, and screening of research subjects
  • Demonstrated experience with the management and design of protocols, data gathering, and evaluation
  • Demonstrated experience taking patient history, evaluating patient problems and providing accurate and complete documentation in patient record
  • Demonstrated experience collecting, evaluating, and interpreting routine standard lab tests on human subjects, i.e. blood tests, vital signs. Ability to read and interpret lab results and summarize scientific data
  • Organizational skills with the ability to prioritize workload effectively and efficiently to meet firm deadlines in an environment with multiple interruptions and changing priorities while exercising independent judgement, showing initiative and resourcefulness when making decisions
  • Strong interpersonal, as well as written and verbal communication skills (using grammatically correct written English and accurate typing) to interact with a variety of personalities at all levels of the organization, exercising tact, mature judgment, diplomacy, and flexibility to promote positive working relationships and job effectiveness. Skill at negotiating with various personalities and developing internal and external network of contacts. Excellent phone etiquette skills
  • Computer proficiency, including word processing, spreadsheet software and internet browser applications. Thorough database management skills
  • Experience with cost accounting as applied to both University and Medical Center functions. Demonstrated knowledge of medical billing and collections guidelines and procedures
  • Experience in data analysis and presentation
  • Knowledge of and ability to operate various industry programs and vendor software
  • Experience reading and interpreting EKGs
  • Experience working in a cardiology department/setting
9

VAD Clinical Research Coordinator Resume Examples & Samples

  • Outline your service excellence, communications and event planning skills and experiences which would be applicable to this position
  • Describe your key impressions of the FCVC presentation found here
  • Assist with the recruitment and retention of subjects, scheduling of procedures, and collection of data. Track visits ensuring compliance with protocol requirements
10

Clinical Research Coordinator Ii Neurology Days Msh Resume Examples & Samples

  • Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects
  • Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests
  • Knowledge of standard concepts, practices and procedures in directly related field
11

Clinical Research Coordinator Cardiology Resume Examples & Samples

  • Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, providing support to the Principal Investigator
  • Assists in the activities related to clinical research including, but not limited to: obtaining informed consent, screening participants for eligibility, registering patients with sponsoring agencies, administering questionnaires and answering telephone calls
  • May assist in the preparation for regulatory agency site visits
12

VAD Clinical Research Coordinator Resume Examples & Samples

  • Describe your key impressions of the FCVC presentation found here: www.med.umich.edu/cv...cvcpotentialteam.pdf
  • Maintains accurate research records and transcribes collected data onto source documents and electronic case report forms. Upload images, request records, and file documents appropriately for audit readiness
  • Assist with identification, documentation and reporting of adverse events according to standard operating procedures and protocol requirements
  • Assists with writing, editing, and renewing Institutional Review Board applications; maintain version trackers for IRB applications, informed consent documents, protocol version trackers, and other related items
  • Assist with budget and billing calendar development and revisions. Review account statements comparing against payment schedule and billing calendar to ensure accuracy. Prepare and submit requests for billing adjustments and invoices as needed. Maintain revenue tracker and assist with budget forecasting
  • Assures compliance with protocols, adherence to good clinical practice guidelines, FDA regulations, and all other federal, local, and University guidelines
  • Perform study-specific tests in clinic such as mini-mental, grip test, and walk test
  • Other duties as assigned or required for the research project
  • Some weekend coverage hours are anticipated during study enrollment period
  • Some overnight travel expected for study related meetings and conferences
13

Clinical Research Coordinator, CRC Resume Examples & Samples

  • Partner with members of the Operations and Research teams to play an active role in ensuring the success of Company-led research studies
  • Lead the preparation of clinical protocols, amendments, informed consent forms, study guides, case report forms, and any other clinical research related documents
  • Monitor performance of investigational sites
  • Educate study sites in correct collection, processing and shipping of biospecimens to central repository
  • Closely monitor study subjects' progress, document research observations, and assess the need for action and/or consultation with the Manager of Clinical Research Operations
  • Act as the voice of the Company with study participants and other external partners
  • Interact with potential study participants, educating them about the study including the possible risks/benefits, procedural details and significance of the study; answers study related questions posed via e-mail or phone calls from potential participants and/or the general public
  • Data collection and data entry, including performing regular audits to ensure that the data collected is complete and accurate
  • Assist with the production of participant education material, research newsletters, development of web content and online project communication
  • Communicate progress and research findings with regular presentations
  • Handle various administrative activities generally associated with conducting research studies
  • Bachelor’s Degree in business administration, health care administration or related field
  • Minimum of two years of experience in clinical research
  • Experience working on a research study with a biobank component strongly preferred
  • Passionate about Clinical Studies
  • Strong organizational, and communication skills
  • Energetic and self-motivated
  • “Think outside of the box” mentality
  • Driven to meet ongoing research milestones
  • Strong problem-solving skills and willingness to go the extra mile to get the job done
  • Ability to efficiently acquire new technical skills or domain expertise
  • Positive attitude and is open to close collaboration within a dynamic and driven team
14

Per Diem Clinical Research Coordinator Resume Examples & Samples

  • Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff
  • Assesses research subjects including obtaining blood samples through venipunture/finger stick, measuring blood pressure, counseling subjects based on assessment findings
  • Read source documents and enter data in specific data fields accurately
  • Collect, compile, sort and verify the data’s accuracy or completeness before it is entered
  • May perform data integrity tasks by locating and correcting data entry errors, or reporting them to supervisors
  • Bachelor’s in Science or closely related field or equivalent experience
  • Health care background is a plus
15

Clinical Research Coordinator, RN Resume Examples & Samples

  • Reports all serious adverse events to sponsor and IRB of record according to established timelines
  • Coordinates research activities not limited to: scheduling laboratory tests, radiology testing and other medical exams
  • Performs and/or oversees a variety of clinical duties that may include but not limited to: EKGs, processing/shipping of blood serum, urine and communicates results to PI and/or APN
  • Act as principal investigator's representative as appropriate. This may include communicating with sponsors and their representatives, the IRB and other medical personnel
  • Maintains accurate, complete, up-to-date records on each patient participating in a clinical trial protocol
  • Ensures study patient's clinical trial related activities are billed appropriately and reconciles drug study account records with research finance personnel
  • Prepares and assists for sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit
  • Develops case report forms and/or databases for physician initiated studies as needed
  • Assists the principal investigator in preparing for publication. Works with analysts and assists with queries related to data to evaluate the significance of collected data
  • Provides education to all departments and clinical areas where study is performed
  • Attends research meetings and conferences as required
  • Participates in staff meetings and in-service education of nursing and medical staff
  • Adheres to the standards identified in the Medical Center's Organizational Competencies
  • Graduate of a NLN/AACN accredited program in nursing
  • 3-5 years clinical nursing experience
  • Adheres to the American Nurses Association standards
  • Mandatory education on human subjects research
  • FDA regulatory, IND reporting, Microsoft or similar Office Suite, oncology or clinical research
  • NJ State Professional Registered Nurse License
16

Clinical Trials Research Coordinator Resume Examples & Samples

  • Theoretical knowledge of a biological science such as Biology, Microbiology or a related field. Knowledge of the basic science of Gulf War Illness, including familiarity with general medical problems and terminology
  • Excellent organizational skills. Experience planning, organizing, and managing the scheduling of study visits, sponsor visits or teleconferences, and meetings with key personnel, all in the midst of handling multiple priorities and deadlines
  • Excellent communication skills. Ability to quickly comprehend written and oral instructions. Ability to write legibly to complete data collection forms. Ability to work effectively as a team member
  • Knowledge and skill in using Microsoft applications including Word, Excel, PowerPoint, and Outlook, as well as research databases, electronic case report forms, and other computer based programs. Ability to organize and concurrently manage information in several formats: paper, electronic, and oral
  • Experience developing complex surveys that require skip and other forms of logic while utilizing survey-based software
  • Experience with Qualtrics
  • Experience coordinating clinical trials in a diseased population with multiple health problems. Ability to read scientific text for general understanding of basic concepts. Ability to summarize and convey technical and medical information to lay individuals at a level appropriate for their understanding
  • Knowledge of common laboratory tests performed and associated normal results
  • Familiarity with regulatory documents needed for the conduct of clinical trials. Experience in submitting applications, consents and correspondence to the IRB and/or UCSD Human Research Protections Program for review and approval
  • Knowledge in the processing and shipping of blood and urine laboratory specimens, both ambient and frozen. Familiarity with guidelines of biohazardous handling. Knowledge and strict utilization of universal precautions when handling laboratory specimens
  • Familiarity with electronic medical records (Epic preferred) for reviewing hospitalizations, laboratory results, and other clinical data
  • Familiarity and comfort in communicating with patients with acute and chronic health problems. Ability to advocate for subjects if their understanding of the nature of their study participation is in question
17

Clinical Trials Research Coordinator Resume Examples & Samples

  • Study Implementation
  • Maintain the security & confidentiality of participants' paper or electronic data (e.g., case report forms kept in a secure, locked space). Assist w/ scheduling participants for study assessments/visits, required tests including visit-specific laboratory kits and/or paperwork preparation. Prepare packets for participants (e.g., instructions, phone numbers, calendars, diaries, etc.)
  • Prefer experience with Excel, Microsoft word, & internet use
  • Preferred one plus years experience in cancer research and or adult oncology
18

Temporary Assistant Clinical Research Coordinator Resume Examples & Samples

  • Schedule and/or call subjects to confirm appointments; contact participants with reminders or other requirements
  • Prepare, distribute, and process questionnaires
  • Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence
  • Prepare, process, and ship specimens/samples accurately under-defined requirements
  • Order and maintain equipment and supplies
  • Process study compensation payments and thank you letters to subjects upon completion of trial activities. Assist with post-study activities, as needed
  • General knowledge of medical terminology
  • Excellent customer service and interpersonal skills
19

Clinical Research Coordinator Dept of Surgery Resume Examples & Samples

  • Assists in the collection, analysis and review of experimental data for publication and presentation
  • Ensures accurate, confidential and complete compilation of data
  • May secure and ship clinical specimens as required by the protocol
20

Clinical Research Coordinator Hal-biltmore Resume Examples & Samples

  • 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
  • Provides a safe environment for patients, families, and clinical staff at all time 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
  • HEC
21

Rn-clinical Research Coordinator Resume Examples & Samples

  • Maintains investigational drug accountability
  • Schedules and participates in monitoring and auditing activities
  • Participates in required training and education programs
  • 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
  • Minimum one (1) year of experience in a clinical or scientific related discipline, preferably in oncology
  • Proficiency in MS Programs such as Word, Excel, and Outlook
  • Good communication
  • Organized
  • Independent
  • Time management
22

Clinical Research Coordinator Supervisor Resume Examples & Samples

  • Clinical Trial Professional certification from a professional society must be obtained within one year of position
  • Demonstrated management and conflict resolution skills to effectively lead and motivate others
  • Demonstrated experience in training others in the field of research
23

Clinical Research Coordinator Supervisor Resume Examples & Samples

  • Clinical Trial Professional certification from a professional society within one year in position
  • Demonstrated experience managing people with a wide range of educational backgrounds and skills. Demonstrated management and conflict resolution skills to effectively lead and motivate others. Demonstrated experience in training others in the field of research
  • Ability to perform all commonly applicable functions in word processing and spreadsheet software; effectively use campus' clinical information and documentation application programs. Proven ability utilizing clinical trial management systems
24

Research Coordinator, Clinical Trials Office Resume Examples & Samples

  • Ability to function independently and as part of a team
  • Excellent communication skills, verbal and written
  • 2 years of clinical experience in a healthcare setting required
  • Demonstrable computer competency in Microsoft Word and Excel
  • Certification by the Association of Clinical Research Professionals preferred
25

Oncology Clinical Research Coordinator Days CHI Health Cumc Bergan Mercy Resume Examples & Samples

  • Recruits, screens, enrolls and obtains consent from program participants
  • Promotes use of open and available clinical studies to appropriate health care providers and venues
  • Conducts and/or coordinates training for program participants
  • Assures compliance with all relevant IRB and other regulatory agency requirements
  • Serves as subject matter expert for all phases of the research trials as assigned
  • Collects, manages and maintains patient and laboratory data for clinical research studies
  • Analyzes and abstracts data from departmental and medical record charts to complete and submit case report forms
  • Maintains and tracks computerized database registration of required research subject data, including demographics, clinical, laboratory and tracking data
  • Verifies research subject eligibility, required tests, therapy, health status, toxicity modifications, etc
  • Coordinates collection and shipment of required specimens for protocol if applicable
  • Participates in audits of assigned protocols
  • Participates in all mandatory quality improvement, safety, security, and infection control program
  • Sound understanding of the treatment options available to individuals with health conditions related to the area of research the incumbent will support. Knowledge of how to conduct research is preferred
  • Has command of verbal and written communication skills and is detailed oriented with data management and protocol execution
  • Proficient in balancing multiple study protocols, risk management procedures, and quality improvement initiatives
  • Communicates effectively with a variety of departments, physicians and staff
  • Maintains strict participant confidentiality, adheres to ethical principals in the conduct of research, and able to prioritize research case load
  • Able to work independently, be organized and manage time effectively
26

Bruog Clinical Research Coordinator Resume Examples & Samples

  • Prior experience working on clinical research trials a plus
  • Knowledge of some medical terminology required; Oncology terminology preferred
  • Prior knowledge and training with an electronic database system a plus, or proficiency in learning a computerized data system
  • Ability to work independently and good time management skills
  • Detail orientation is critical to this job
27

Certified Clinical Research Coordinator RN Resume Examples & Samples

  • Protocol Guidelines: With PI and CRC, develop Standard Operating Procedures (SOPs), “Patient Study Calendars”, Orders, and Eligibility Checklists for all new studies. Must be fully knowledgeable of the specifics of the protocol and ensure that written guidelines are in place. For PI-initiated trials, will work with PI to develop Case Report Forms (CRFs) as well
  • Liaison with Clinical Departments/Units: Act as liaison with Pharmacy to ensure the investigational drugs are available for protocol. Liaison with Laboratory and/or other hospital ancillary departments as needed
  • Protocol Training (In Servicing): Train hospital/practice personnel in the specifics of the trial
  • Enrollment of Patients: Identify patients for that meet criteria for protocol. Screen, consent and reconsent patients for study
  • Monitoring Visits/Audits: Act as protocol representative during visits from monitors or auditors
28

Clinical Research Coordinator, Ophthalmology Resume Examples & Samples

  • Coordinate research protocols; arrange necessary appointments and procedures, collect required data, work collaboratively with other departments and institutions, and maintain contact with study participants
  • Recruit, screen, enroll and obtain consent from study participants
  • Organize and maintain study documents including data collection forms, informed consent forms, and regulatory documents
  • Maintain timelines, including tracking deadlines for program components
  • Provide back-up coverage for refractions and visual acuity measurements in accordance with varying research protocols; maintain required certifications
  • Enter data into electronic data capture (EDC) systems
  • Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study team
  • Perform ancillary testing including vital signs, intraocular pressure measurement, visual field measurement, optical coherence tomography (OCT), color vision testing, and other basic ophthalmic photography; administer surveys
  • Assist with the preparation of IRB documents and reports
  • Assist with the collection of patient samples, including blood, urine, and saliva; process and prepare specimens (centrifuge, pipette as required)
29

Clinical Research Coordinator Clinical Trials Unit Women s Health Resume Examples & Samples

  • Current Basic Life Support (BLS) certification from the American Heart Association
  • 6 years relevant research experience in a clinical setting or 3 years of research experience in a clinical setting with a Bachelor of Science degree
  • Experience working independently, organizing work, and setting priorities
  • Must have computer skills and dexterity required for data entry and retrieval of information
30

Clinical Research Activation Coordinator Resume Examples & Samples

  • Manage the processes required for identification, assessment, submission and initiation of clinical research studies at the Massey Cancer Center in collaboration with all members of the research team
  • Identifies potential clinical trials to fill out protocol menu
  • Manages and designs systems to identify, evaluate, and usher new clinical trials through the activation phase
  • Interface with clinical investigators, trial sponsors and others involved in the clinical research process
  • Develop, establish and maintain productive relationships with VCU colleagues and customers to achieve essential clinical research outcomes
  • Meets directly with investigators, regulatory, and administrative supervisors and team members
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Qualitative Clinical Research Coordinator Resume Examples & Samples

  • Communicate effectively across interdisciplinary project teams across institutions, to include project updates, pending tasks, and team meetings
  • Prepare, coordinate and track materials for all initial, modification and continuing review IRB submissions
  • Review literature and synthesize findings on a variety of child health topics
  • Develop, maintain, and update data collection instruments (e.g. interview guides, surveys) for research purposes
  • Assist project team with data collection, management, and analysis
  • Conduct interviews and focus groups with research study participants
  • Create and manage NVivo project files among team members
  • Perform analyses using NVivo query functions and memoing in preparation for team meetings, under direction of lead investigators
  • Participate in conversations with multidisciplinary team members concerning the research process and future directions to ensure high quality and high impact research
  • Assist in all aspects of preparation of scientific manuscripts for submission to peer reviewed journals
  • Apply relevant project lessons and skills to ongoing PolicyLab initiatives
  • Bachelor's degree with two (2) - five (5) years of public health research experience OR Master's Degree in Public Health or Social Work with one (1) - 3 (3) years of public health research experience
  • Experience with NVivo or equivalent Qualitative Data Analysis software required
  • Masters degree in Public Health (or related field) with at least 3 years clinical research experience
  • Pediatric clinical research and CDE preferred
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Clinical Research Coordinator Hoag Inst for Research & Ed Resume Examples & Samples

  • Assist the Principal Investigator (PI) in the conduct of the clinical study according to FDA and Sponsor regulations and guidelines and ensures the safety and welfare of the research participants
  • Designs, implements and manages a system for organizing, planning work flow related to all research study activities. Prepares and presents summary of clinical trial activities if needed
  • Be knowledgeable of study protocols to complete study activities correctly and completely. Design and/or maintain organizational tools to conduct the study accurately and in compliance with Good Clinical Practice. Develops forms, check-lists and other tools to facilitate study completion and compliance
  • Assist the PI in the active recruitment and screening of potential research participants according to the protocol’s inclusion/exclusion criteria. Schedule research participant’s visits in accordance with 1 study protocol. Assist the PI in the training of other site personnel and other medical staff in understanding and implementing the protocol
  • Drafts or reviews template Informed Consent Forms with Clinical Research Office per FDA, ICH, GCP guidelines and Hoag Policy language
  • Discusses research study with potential research participants and answers any questions while coordinating the process of obtaining the research subjects informed consent prior to participation in the study. . The CRC shall seek guidance from the Principal Investigator for any questions he/she cannot accurately answer for the research participant regarding the study or participant’s medical condition
  • Schedule or assist in scheduling follow-up visits for enrolled subjects
  • Documents and reports Unanticipated Problems, Adverse Events and Serious Adverse Events according to Clinical Research Office policy, Sponsor, IRB, FDA, ICH and GCP guidelines and specific protocol, to the Investigator, Sponsor, Clinical Research Office administrative staff, and IRB
  • Complete the Case Report Forms for the study accurately and completely. Abstract data from hospital record and physician charts to complete CRFs
  • Work with ancillary staff areas (e.g. Operating Nursing Care, Cath Lab, Pharmacy, Pathology, Radiology, Laboratory, Medical Records) within the hospital affected by research activities
  • Maintain accurate and complete records of the receipt, dispensing, and return of all investigational supplies, including study drug(s) or devices, and report any discrepancies to the PI and Sponsor
  • Maintain required regulatory and other documentation in the study documentation file. Maintain records of research participants enrolled in the study
  • Communicate with the study sponsor regarding study activities as necessary. Participates in required study visits such as Initiation Visit, Routine Monitoring Visits, Close-out Visits and audits. Reviews study records and meets with site visit teams/monitors, the FDA, or other inspectors as designated by sponsor when required. Resolves queries generated from Sponsor or other monitoring/auditing reports
  • Completes study Institutional Review Board submission application and ensures Investigator's review. Communicate with the designated IRB on study approvals/closures, and adverse event reporting
  • Work with the Clinical Research Office (CRO) administrative staff on all required aspects of study submission, continuing reviews, adverse event reporting, and study closure. Maintains current knowledge of Clinical Research Policies and Procedures
  • Works with Clinical Research Office administrative staff in developing a detailed cost analysis, study budget preparation, and tracking/distribution of study funds
  • Accommodates changes in workload within the department and demonstrates flexibility in accepting work assignments. Performs assignments as directed by Supervisor
  • AA degree
  • Minimum 1 (one) year of Clinical Research Coordinator experience
  • Patient coordination experience in complex clinical trial setting required (does not include Regulatory position)
  • Medical terminology required
  • Working knowledge of FDA, NIH and OHRP regulatory requirements and ICH GCP guidelines. Understanding of clinical trial methodologies and experience filing Institutional Review Board documents
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VAD Clinical Research Coordinator Resume Examples & Samples

  • Describe your key impressions of the FCVC presentation
  • Certification through ACRP or SOCRA or willingness to become certified
  • Demonstrated knowledge of medical and research terminology and familiarity in heart disease
  • Knowledge of preparation of regulatory documents for clinical trials for submission to IRB (eResearch)
  • Ability to work with minimal supervision with diverse teams of people in a diplomatic, collaborative and effective manner
  • Excellent interpersonal, oral, and written communication skills with exceptional attention to detail
  • Exceptional organizational and computer skills are required with proficiency in Microsoft software applications
  • Demonstrated problem solving and conflict resolution skills
  • Ability to multi-task, work well under time constraints and meet deadlines
  • Demonstration of commitment to FCVC Core Values
  • Previous experience of 1-2 years with coordination and management of device trials (IDE and HDE) desired
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OPS Clinical Research Coordinator Resume Examples & Samples

  • Experience working with ICU patients
  • Familiarity for medical terminology
  • Knowledge of basic anatomy