Clinical Research Coordinator III
About The Position
The primary responsibility of the Clinical Research Coordinator III is to coordinate and conduct all aspects of a clinical study, with minimal supervision from the investigators. The Clinical Research Coordinator III is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. The Clinical Research Coordinator III assists the investigator team to develop study protocol and manuals of procedures. As the primary resource for the protocol, the Clinical Research Coordinator III acts as a liaison between the patient, investigator, collaborators, and Institutional Review Board. The Clinical Research Coordinator III also serves as a resource for other staff members. The Clinical Research Coordinator III screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive tests according to study protocols. The Clinical Research Coordinator III is also responsible for keeping all data and source documentation, adverse event reporting, and IRB regulatory files.
Requirements
- Bachelor’s Degree or RN with current state licensure at the time of hire and two (2) years of related work experience; OR LPN with current state licensure at the time of hire and five (5) years of related work experience; OR Master’s Degree in a related field and one (1) year of related work experience.
- In-depth knowledge of protocol requirements and good clinical practices.
Nice To Haves
- Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA) is strongly desired.
- Supervisory experience is preferred.
Responsibilities
- Coordinate and conduct all aspects of a clinical study.
- Assist the investigator team to develop study protocol and manuals of procedures.
- Act as a liaison between the patient, investigator, collaborators, and Institutional Review Board.
- Serve as a resource for other staff members.
- Screen, enroll and follow study participants.
- Conduct data collection and entry.
- Perform noninvasive tests according to study protocols.
- Keep all data and source documentation.
- Report adverse events.
- Maintain IRB regulatory files.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
