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Job Description
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’ 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.