Clinical Research Associate - FSP - Czechia
Core
Coordinate clinical monitoring and site management to ensure trials comply with protocols, ICH-GCP guidelines, and regulations, guaranteeing subject rights and data reliability.
Role type
Level II Clinical Research Associate (FSP)
Builds
Clinical trials for pharmaceutical and biotech sponsors
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Risk-based monitoring, root cause analysis, protocol compliance, ICH-GCP knowledge, site initiation, trial close-out, data review (SDR/SDV/CRF), investigator payment processing
Preferred skills
Medical/therapeutic area knowledge, Clinical Trial Management System proficiency
Technologies
Clinical Trial Management Systems, Microsoft Office
Responsibilities
Monitor investigator sites using risk-based approaches to identify and resolve compliance issues; initiate and close out clinical trial sites; conduct on-site file reviews; track study progress and update systems; facilitate communication between sites, clients, and project teams; respond to audits and inspections.
Seniority
Mid-level, hands-on IC