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Clinical Trial Coordinator

Thermo Fisher Scientific

New
Onsite Junior 🇬🇧 English
MS Office Activate eTMF CTMS

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.

Questions fréquentes

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Published 13 hours ago

Expires 1 month from now

5 views · 0 interested

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Thermo Fisher Scientific