Description
Join IQVIA Biotech as a Freelance Clinical Research Associate supporting two Phase III Oncology clinical trials. You'll lead site visits, monitor compliance, and ensure high-quality data,all while working with a team.
Your Role
- 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
Your Profile:
- 2+ years CRA including site monitoring experience
- Oncology/Hematology experience
- Strong knowledge of clinical trial processes & GCP
- Excellent communication & organisational skills
- Ability to work independently and manage priorities
- Fluent in Czech and English
If you're ready to make an impact in clinical research, apply today!