Coordinate daily operational activities across multiple research studies.

Serve as the primary contact between site research teams, sponsors, and supervisors.

Collaborate with internal departments such as finance, administration, and the local IRB.

Manage study timelines from feasibility submission through study closeout.

Review study design, inclusion/exclusion criteria, and ensure accurate informed consent.

Maintain data integrity through detailed source document review and accurate data entry.

Create study-specific documentation tools when not provided by sponsors.

Manage shipment tracking for drugs, devices, and study supplies.

Document and report adverse events, deviations, and protocol violations.

Attend ...