Proclinical is working closely with a healthcare organization who is seeking a dedicated Clinical Research Associate to join their team. The successful candidate will play a crucial role in determining study eligibility, obtaining study consent, scheduling study procedure visits, and coordinating the collection and processing of study specimens. This role requires a meticulous individual who can review medical records, compile data, and interpret clinical data under investigator supervision.
Key Responsibilities
Determine study eligibility and obtain study consent for clinical trials.
Schedule study procedure visits as per study protocol.
Coordinate the collection and processing of study specimens.
Review medical records and compile data into the sponsor-provided database.
Interpret clinical data, including adverse events and drug response, under investigator supervision.
Prepare required study protocol documents for submission to the Institutional Review Board (IRB).
Establish and organize study files, including regulatory binders and study-specific source documents.
Serve as the primary contact with research subjects and sponsors.
Work on multiple studies simultaneously.
Requirements
Ability to work in-person weekdays from 8am-4:30pm.
Willingness to rotate on-call duties as needed per study-specific enrollment.
Flexibility to rotate work in the Transplant Clinic to complete subject study visits.
Ability to manage multiple tasks and studies at one time.
If you are having difficulty in applying or if you have any questions, please contact Natalie Magola at n.magola@proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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