FSP Clinical Research Associate II/Senior Clinical Research Associate - Czechia
Thermo Fisher Scientific · Remote
Clinical OperationsRemoteFull timeCompany career page
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Role summary
Thermo Fisher Scientific seeks a Clinical Research Associate II to conduct remote and on-site monitoring of investigational sites across clinical trials. The role involves assessing protocol compliance, managing documentation, and ensuring data integrity while collaborating with sponsors and sites.
What they're looking for
- Bachelor's degree in life sciences or registered nursing certification
- Approximately one year clinical research monitoring experience or PPD Drug Development Fellowship completion
- Proficiency in ICH-GCP guidelines and applicable regulatory requirements
- Strong critical thinking and root cause analysis skills for problem-solving
- Excellent written and oral communication abilities
- Risk-based monitoring expertise and organizational skills
What you'll be doing
- Conduct remote and on-site site visits to assess protocol and regulatory compliance
- Perform source document review, SDR, SDV and CRF verification activities
- Initiate and close out investigational sites while managing essential documentation
- Prepare monitoring reports and escalate deficiencies to clinical management for resolution
- Maintain communication with investigative sites and provide trial status updates to project teams
Privacy & handoff
This role links to Thermo Fisher Scientific'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.