FSP Clinical Trial Coordinator
Thermo Fisher Scientific
Thermo Fisher Scientific seeks a Clinical Trial Coordinator to support clinical operations across multiple trials. The role involves administrative and technical support for site activation, file management, regulatory compliance, and coordination with internal teams and investigator sites.
Responsibilities
- Coordinate site activation activities and develop critical paths for rapid site onboarding
- Perform file reviews and audits according to SOPs; document findings in designated systems
- Manage electronic trial master file (eTMF) and system databases; process documents for client submission
- Develop and review investigator site lists for feasibility activities and site tiering
- Analyze study metrics, reconcile findings reports, and assist with resolution of documentation issues
Requirements
- High school diploma or equivalent; bachelor's degree preferred
- 0-1 year relevant experience in clinical operations or related field
- Strong organizational skills and attention to detail
- Ability to analyze project data and systems for accuracy
- Flexibility to manage shifting priorities and multiple concurrent tasks
- Team collaboration and independent work capability
- Customer-focused approach and regulatory knowledge
Vacancy posted 6 days ago
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