CRA I/CRA II
Fortrea · Warsaw, Poland
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Fortrea seeks Clinical Research Associates to manage clinical trial sites and conduct monitoring activities according to ICH GCP guidelines and SOPs. Responsibilities include site initiation, data verification, regulatory compliance, and investigational product accountability. The role requires independent monitoring capability and frequent travel.
What they're looking for
- University degree or allied health certification (e.g., nursing licensure)
- Minimum 2 years of clinical monitoring experience
- Fluent in Polish and English, written and verbal
- Thorough knowledge of ICH GCP guidelines and local regulatory requirements
- Ability to work independently with minimal supervision
- Understanding of serious adverse event reporting and clinical trial processes
- Strong planning, organization, and problem-solving abilities
What you'll be doing
- Conduct site monitoring visits including pre-study, initiation, routine, and close-out activities per SOPs
- Perform source document verification, eCRF review, query generation and resolution
- Verify informed consent procedures, protocol adherence, and subject protection measures
- Manage investigational product inventory, accountability, and secure storage
- Prepare trip reports, monitoring plans, and maintain trial management systems
Privacy & handoff
This role links to Fortrea's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.