Manager/Associate Director, Medical Writing - Regulatory
Clinical Careers Page(12 days ago)
About this role
This role involves leading medical writing teams within the regulatory sector at Syneos Health. It includes overseeing project management, ensuring quality compliance, supporting business development, and participating in document development strategies.
Required Skills
- Medical Writing
- Regulatory Documentation
- Team Leadership
- Quality Assurance
- Project Management
- Cross-functional Collaboration
- Budgeting
- Medical Affairs
- Clinical Development
- SOP Development
About Clinical Careers Page
syneoshealth.comSyneos Health is a biopharma solutions organization and full‑service contract research organization (CRO) that integrates clinical development, regulatory and commercialization services to help life‑science companies bring therapies to market faster. It provides end‑to‑end capabilities — clinical trials across phases and therapeutic areas, real‑world evidence and data analytics, medical affairs, market access, patient engagement and commercial launch services. With a global network of scientific, clinical and commercial experts, Syneos partners with biopharma, biotech and medtech clients to de‑risk development programs and accelerate product adoption.
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