Site Coordinator
Core
Support clinical trial sites in all related activities according to ICH-GCP and protocol requirements to meet enrollment goals.
Role type
Site Coordinator
Builds
Clinical trial data and regulatory compliance for medical institutions
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
ICH-GCP knowledge, patient enrollment tracking, EDC data entry, adverse event reporting, investigational product handling, regulatory document management, contract negotiation support, audit preparation
Preferred skills
Pharmacy, nursing, or lab analytics background, global team collaboration
Technologies
EDC systems
Responsibilities
Act as main communication line between Sponsor/CRO and site, assist in scheduling monitoring visits, track patient enrollment, maintain study documents, enter data into EDC systems, report adverse events, handle investigational products, prepare for audits, support contract negotiations
Seniority
Mid-level, hands-on IC
