Clinical Site Coordinator
Core
Support clinical trial sites in Serbia with all related activities according to ICH-GCP and protocol requirements.
Role type
Clinical Site Coordinator
Builds
Clinical trial operations for medical institutions and research centers
Domain
Clinical research / Life Sciences
Deliverable
client delivery
Required skills
ICH-GCP compliance, patient enrollment tracking, EDC data entry, adverse event reporting, investigational product handling, regulatory document management, contract negotiation support, audit preparation
Preferred skills
Clinical terminology knowledge, medical research experience, problem-solving in fast-paced environments
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 and protocol deviations; handle investigational products; collect regulatory documents; support contract/budget negotiations; prepare for audits/inspections
Seniority
Mid-level, hands-on IC
