Under general supervision, the Clinical Research Coordinator (CRC) - Intermediate champions patient safety and protocol integrity while upholding the highest standards of patient care. The CRC communicates effectively to support the successful conduct of clinical trials and ensure quality outcomes. Responsibilities include screening and scheduling patients, coordinating all on-study activities, and maintaining compliance with study requirements. The CRC also participates in study teleconferences with sponsors and clinical research organizations to promote clear communication and continuity of information.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed