Clinical Trial Coordinator
Thermo Fisher Scientific
Job description
About the role
Join a global team supporting leading pharmaceutical companies and biotechs. As a Clinical Trial Coordinator you will provide administrative and technical support to project teams, ensuring audit readiness and efficient site activation.
Key responsibilities
- Coordinate and oversee assigned trial activities, performing file reviews and documenting findings.
- Provide system support for Activate and eTMF, ensuring databases are current and documents are processed timely.
- Assist with site activation tasks, including preparation of Investigator Site Files, pharmacy binders, and regulatory submissions.
- Analyze study metrics, reconcile findings, and support risk communication to project leads.
Required profile
- High school diploma or equivalent; bachelor’s degree preferred.
- 0‑1 year relevant experience or equivalent combination of education and training.
- Strong organizational skills, attention to detail, and ability to manage multiple tasks.
Required skills
- Proficiency in MS Office (Word, Excel, PowerPoint).
- Experience with clinical trial systems such as Activate, eTMM, and CTMS.
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Published 13 hours ago
Expires 1 month from now
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Thermo Fisher Scientific