Clinical Site Coordinator
Core
Supports a Clinical Study Site in clinical trial related activities according to ICH-GCP and protocol requirements.
Role type
Clinical Site Coordinator
Builds
Supports clinical study sites in stronger study delivery
Domain
Clinical trials / Life Sciences
Deliverable
client delivery
Required skills
ICH-GCP compliance, patient enrollment tracking, data entry into EDC systems, adverse event reporting, investigational product handling, regulatory document management, contract negotiation support, audit preparation
Preferred skills
Degree in Life Science (pharmacy, nursing, or lab analytics), 2+ years of on-the-job experience as a site coordinator
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; support contract negotiations; prepare for audits
Seniority
Entry-level to Mid-level, hands-on operational role
