Site Coordinator
Core
Support clinical study sites in trial activities including patient enrollment, data entry, regulatory document management, and investigational product handling.
Role type
Site Coordinator (Clinical Trials)
Builds
Clinical trial data and regulatory compliance for pharmaceutical/biotech studies
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Patient enrollment tracking, EDC data entry, adverse event reporting, investigational product reconciliation, regulatory document management, audit preparation, contract negotiation support, scheduling study procedures
Preferred skills
Background in pharmacy, nursing, or lab analytics
Technologies
EDC systems
Responsibilities
Act as main communication line between Sponsor/CRO and site; Track patient enrollment and support meeting timelines; Maintain study documents and ensure accurate data entry; Report adverse events and protocol deviations; Handle investigational products; Prepare for audits and inspections
Seniority
Mid-level, hands-on IC
