Clinical Site Coordinator - Part Time
Core
Support clinical study sites in trial activities including monitoring visits, patient enrollment, data entry, and regulatory document management.
Role type
Clinical Site Coordinator
Builds
Clinical trial operations at medical institutions
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Patient enrollment tracking, EDC data entry, adverse event reporting, investigational product handling, regulatory document management, audit preparation, contract negotiation support, scheduling study procedures
Preferred skills
Pharmacy, nursing, or lab analytics background
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
Seniority
Individual Contributor, 2+ years experience