Freelance CRA - Czech Republic
Core
Lead site visits, monitor compliance, and ensure high-quality data for Phase III Oncology clinical trials.
Role type
Freelance Clinical Research Associate (CRA)
Builds
Clinical trial data integrity and regulatory compliance for oncology studies
Domain
Life sciences / Clinical research / Oncology
Required skills
Site monitoring, GCP compliance, Protocol review, Investigational product inventory management, Audit readiness support
Preferred skills
Oncology/Hematology experience, Independent work management
Technologies
eCRFs, Study manuals
Responsibilities
Conduct site evaluations, initiations, monitoring & close-outs; Ensure GCP compliance and data integrity; Collaborate with investigators and internal teams; Review protocols, study manuals, and eCRFs; Support site staff with training and issue resolution; Track investigational product inventory and documentation; Attend investigator meetings and study-related events; Contribute to audit readiness and inspection support
