Clinical Research Associate I
Thermo Fisher Scientific · Remote
Clinical OperationsRemoteFull timeCompany career page
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Role summary
Thermo Fisher Scientific seeks a Clinical Research Associate to conduct remote and on-site monitoring of clinical trial sites. The role involves assessing protocol compliance, managing documentation, and ensuring data integrity across multiple sponsor environments and regulatory frameworks.
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 with ICH-GCP guidelines, regulations, and risk-based monitoring approaches
- Strong critical thinking, root cause analysis, and problem-solving capabilities
- Excellent written and oral communication skills with medical professionals
- Demonstrated attention to detail and organizational abilities
What you'll be doing
- Conduct risk-based site monitoring visits to assess protocol and regulatory compliance
- Review source documents, case report forms, and investigational product records for accuracy
- Document observations and escalate deficiencies to management with timely resolution follow-up
- Initiate and close out clinical trial sites while ensuring essential documents and files are complete
- Facilitate communication between investigative sites, sponsors, and project teams regarding trial status and updates
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.