Clinical Research Coordinator (Onsite)

Coordinate daily operations of research studies from feasibility through closeout.

Act as liaison between site personnel, sponsors, and supervisors.

Collaborate with finance, hospital administration, and IRB (if applicable).

Schedule and track assessments and study milestones.

Ensure proper informed consent and adherence to protocol and regulatory standards.

Enter and verify clinical data in Case Report Forms or electronic systems.

Create source documentation tools when not provided by sponsors.

Monitor and report adverse events, protocol deviations, and waivers.

Manage study supplies, including drug and device shipments.

Attend investigator meetings, site visits, audits, and t...