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CTC - FSP

Fortrea · Chodov, Czechia

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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

Fortrea seeks a Clinical Trial Coordinator to support global clinical trial operations in Prague. The role involves administrative and operational assistance to study teams, including documentation management, logistics coordination, and stakeholder collaboration.

What they're looking for

  • Associate degree or equivalent qualification in relevant field
  • Minimum one year clinical research administrative experience
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Strong written and verbal English communication skills
  • Detail-oriented with excellent organizational abilities
  • Experience in pharmaceutical, clinical research, or CRO industry

What you'll be doing

  • Support coordination and tracking of clinical trial activities and documentation
  • Maintain Trial Master File systems and study tracking records
  • Coordinate study materials, supplies, and logistics management
  • Assist with Investigator Meetings and project communications
  • Collaborate with study teams, sites, sponsors, and external vendors

Privacy & handoff

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What RoleLantern checked

This role is listed from an approved source. RoleLantern checks that the application link is live and how recently the role appeared — the employer has not confirmed it directly on RoleLantern.

RoleLantern checked active
RoleLantern checkedNeeds clarity
Date posted4 days ago
Last source checkToday
Salary listedNeeds clarity
Location clearClear
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