Site Coordinator
Core
Support a Clinical Study Site in clinical trial related activities according to ICH-GCP and protocol requirements.
Role type
Clinical Site Coordinator
Builds
Clinical trial data and regulatory compliance at the site level
Domain
Clinical Research / Life Sciences
Deliverable
physical/clinical work
Required skills
ICH-GCP knowledge, patient enrollment tracking, data entry, adverse event reporting, investigational product handling, document management, audit preparation
Preferred skills
University degree in Life Science (Pharmacy, Nursing, Lab Analytics), 2+ years site coordinator experience, problem-solving in fast-paced environments
Technologies
EDC systems
