Fortrea
Fortrea is a clinical research organization (CRO) with over 30 years of experience dedicated to accelerating the development of life-changing treatments by providing comprehensive clinical solutions for biopharma and MedTech companies. They offer a range of services including clinical trial management, pharmacology services, and regulatory strategy, all designed around the needs of their clients. Fortrea's mission is to put patients at the center of their work, aiming to bring innovative therapies to market faster through tailored, data-driven approaches.
clinical research • clinical trials
10,000+ employees
💊 Pharmaceuticals
Senior Medical Writer
April 8
Fortrea
Fortrea is a clinical research organization (CRO) with over 30 years of experience dedicated to accelerating the development of life-changing treatments by providing comprehensive clinical solutions for biopharma and MedTech companies. They offer a range of services including clinical trial management, pharmacology services, and regulatory strategy, all designed around the needs of their clients. Fortrea's mission is to put patients at the center of their work, aiming to bring innovative therapies to market faster through tailored, data-driven approaches.
clinical research • clinical trials
10,000+ employees
💊 Pharmaceuticals
📋 Description
• Join Fortrea as a Senior Regulatory Medical Writer. • Lead authoring of high complexity clinical regulatory documents for strategic projects. • Spearhead the Development Cycle for Phase II-IV clinical regulatory documents. • Conduct strategy meetings for project goals. • Coordinate with functional leads to ensure document alignment and development. • Critically interpret study data for clear Protocols and CSRs. • Collaborate with teams across Europe and APAC.
🎯 Requirements
• Advanced degree in life-sciences (PhD or Masters) • Minimum 4 years of regulatory medical writing experience, including at least 2 years as medical writing project lead • Extensive experience and proficiency in writing and leading development of CSRs and Protocols
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