Freelance Site Coordinator
Freelance / independent contractor
Core
Support clinical trial sites in all related activities according to ICH-GCP and protocol requirements to meet enrollment goals.
Role type
Freelance Site Coordinator
Builds
Clinical trial data and regulatory compliance for medical institutions/research centers
Domain
Clinical Trials / Life Sciences
Deliverable
client delivery
Required skills
ICH-GCP knowledge, clinical trial terminology, data entry, adverse event reporting, investigational product handling, document management, contract negotiation support, audit preparation
Preferred skills
Life Science degree (pharmacy, nursing, lab analytics), 2+ years clinical trial experience, global team collaboration
Technologies
EDC systems
