Overview The Clinical Research Coordinator (CRC) is responsible for assisting in the planning, coordination, and execution of clinical trials with strict adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), study protocols, and company/regulatory guidelines.

The CRC supports investigators and research teams in ensuring patient safety, data integrity, and compliance throughout the clinical trial lifecycle—from initiation through close-out.   Key Responsibilities Patient Coordination & Support Assist with coordinating all aspects of patient involvement from study initiation through completion.

Schedule participant visits, procedures, and follow-ups according to protocol timelines.

Provide clear communication and education to participants regarding study expectations, informed consent, and potential risks/benefits.

Study Operations & Data Management Organize and maintain all cli...