Clinical Officer – Gilgil at KEMRI

Clinical Officer - Gilgil

• Coordinate and supervise field collection teams and overall field operations.

• Oversee study activities including chart preparation, scheduling protocol-specific procedures, consent administration, SOPs, and training of clinical staff.

• Support the PI in informed consent administration in compliance with study protocols, local regulations, and GCP guidelines.

• Ensure accurate data collection, workflow adherence, data capture in eCRFs/CRFs, and resolution of data discrepancies.

• Monitor study compliance with protocols and GCP; audit study records, source documents, and maintain essential files.

• Document study communications, protocol deviations, adverse events, and maintain regulatory reporting with IRB and investigators.

• Liaise with sponsors, monitors, County Ministry of Health teams, CHMT, CAB, and other partners; prepare for monitoring and close-out visits.

• Support field logistics including supplies, reimbursements, payments, troubleshooting site issues, and preparation of field and progress reports for the PI.

• Any other duties as assigned by PI