Clinical Research Coordinator Jobs description

A clinical research coordinator obtains medical histories and current medications, reviews protocol inclusion/exclusion criteria, confirms the eligibility subjects for studies, and reports to a research manager and team leader. A clinical research coordinator ensures that the informed consent process has been followed, properly documented, and filed as required. A clinical research coordinator schedules subject participation in research, coordinating the availability of necessary space and laboratory and physician support. A clinical research coordinator coordinates with pharmacy staff in dispensing study medication under the direction of the principal investigator and sub-investigators. A clinical research coordinator assures compliance with protocol details, completes necessary records, and coordinates the scheduling of subject and monitoring visits. A clinical research coordinator accurately transfers source documentation into case report form (CRF) within 10 working days and is familiar with all records required for each study, reviewing those records after each visit for completeness and accuracy. A clinical research coordinator collaborates with hospital staff to ensure that the tests and procedures required by clinical protocols are performed and documented. A clinical research coordinator also maintains patients’ clinical research files.

A clinical research coordinator position requires a BS in biology, chemistry, behavioral science, nursing, or a related discipline. A clinical research coordinator should have an aptitude for technical problem solving and the skills required for independent scientific research. A clinical research coordinator should have excellent interpersonal communication skills and the ability to multitask.

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