Senior Compliance Coordinator
Thermo Fisher Scientific · Prague, Czechia
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Role summary
This position supports clinical trial compliance and documentation processes at Thermo Fisher Scientific. The coordinator maintains study records, ensures accurate electronic case report form (eCRF) data entry, manages investigator site files, and assists with quality reviews for low-complexity trials in a Prague office setting.
What they're looking for
- High school diploma or equivalent with relevant formal qualification
- At least 2 years of experience in clinical trials or related field
- Proficiency in Business English, written and verbal
- Basic Microsoft Office and computer skills
- Strong attention to detail and organizational abilities
- Ability to multitask across multiple concurrent studies
What you'll be doing
- Maintain investigator site files and study trackers; verify informed consent forms are properly completed
- Capture and enter source data accurately and timely into eCRF systems
- Verify protocol visit windows comply with requirements and report deviations as quality incidents
- Support data queries, monitoring visits, and escalate unresolved issues to management
- Assist with compliance reporting and adhere to GCP, ICH, and data protection guidelines
Privacy & handoff
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