About this role
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.