Job Description
The Clinical Research Coordinator (CRC) is responsible for the day‑to‑day coordination and execution of clinical research studies conducted under the Clinical Research Center. This role is patient‑facing and requires hands‑on experience coordinating clinical trials, including participant screening, eligibility determination, study visits, and safety reporting.
The CRC will manage 5–10 active studies simultaneously and work closely with Principal Investigators, clinical staff, and research team members to ensure studies are conducted in compliance with protocols, Good Clinical Practice (GCP), and institutional and regulatory requirements. This position requires a minimum of 2 years of direct clinical research coordination experience, beyond monitoring‑only roles.
Key Responsibilities
Study Coordination & Participant Management
Coordinate and conduct study visits according to protocol requirements
Screen and recruit potential study participants, includin...