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.