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healthcare

Posted Apr 10

Clinical Trial Assistant

at Fortrea

Warsaw, PolandOn-site
GCP

Requirements

  • experience as a CTA in a CRO, pharma, or FSP environment Solid knowledge of GCP and clinical trial documentation Strong attention to detail, organization skills, and stakeholder communication 📩 Interested? Apply or get in touch to learn more! Learn more about our EEO & Accommodations request here .

Additional details

  • Fortrea is looking for an experienced Clinical Trial Assistant to support global clinical studies within an FSP model for a leading pharmaceutical sponsor.
  • What you’ll do: Support clinical trials end‑to‑end in close collaboration with Clinical Project Managers and CROs Manage study documentation and eTMF set‑up, maintenance, and reconciliation Support regulatory and ethics submissions, CT.gov maintenance, and trial disclosures Participate in study meetings, CRO oversight activities, audits, and inspections Support CSR approval workflows and eCTD document formatting What we’re looking for: 3+ years’

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