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Clinical Trial Coordinator

Thermo Fisher Scientific · Brussels, Belgium

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Clinical OperationsFull timeCompany career page

RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.

Role summary

Thermo Fisher Scientific seeks a Clinical Trial Coordinator for its Brussels office to support clinical trial operations on a hybrid basis. The role involves coordinating trial activities, maintaining documentation systems, managing regulatory compliance, and liaising across cross-functional teams.

What they're looking for

  • High school diploma or equivalent; bachelor's degree preferred
  • At least 4 years of relevant experience in clinical operations or equivalent combination of education and experience
  • Fluent in Dutch and English; French language skills ideal
  • Strong proficiency in MS Office and ability to master clinical trial database systems
  • Demonstrated knowledge of ICH Good Clinical Practices and country regulatory requirements
  • Excellent organizational skills with ability to manage multiple tasks and prioritize effectively

What you'll be doing

  • Coordinate and oversee assigned clinical trial activities according to role specifications and task matrices
  • Conduct file reviews at department, internal, country, and investigator levels; document findings in appropriate systems
  • Maintain study-specific documentation, electronic Trial Master Files, and project trackers including team lists and training requirements
  • Process documents for client submission, perform regulatory reviews, and coordinate distribution of investigator site files and pharmacy materials to sites
  • Support scheduling of meetings, analyze study metrics, and assist with translation materials and quality control as needed

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Date posted6 days ago
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