Clinical Research Coordinator

Clinical Research Coordinator (CRC)

Key responsibilities typically include :

• Screening and recruiting study participants, verifying eligibility per protocol.
• Conducting informed consent discussions and ensuring ethical treatment of participants.
• Coordinating study visits, executing protocol-specified procedures (labs, vitals, diaries, adverse event monitoring, etc.).
• Monitoring adverse events (AEs) and serious adverse events (SAEs), ensuring timely reporting to sponsors / IRBs.
• Entering data into electronic systems (EDC / CTMS), maintaining source documentation, case report forms (CRFs) and regulatory files.
• Interacting with sponsors / CROs, coordinating with study monitors, handling queries and managing trial logistics.
• Ensuring compliance with Good Clinical Practice (GCP), institutional policies and regulatory requirements.
• Often serving as the participant-facing point of contact and maintaining excellent communication and engagement with subjects and site staff.

Why the role matters :