Senior Medical Writer - CSR and Protocols

Clinical Careers Page(13 days ago)

OnsiteFull TimeSenior$75,000 - $95,000Medical Writing

About this role

A Senior Medical Writer at Syneos Health specializes in creating and coordinating various regulatory and scientific documents for clinical development, ensuring compliance with industry standards and client specifications. The role involves leading writing projects, mentoring junior staff, and collaborating with cross-functional teams to support pharmaceutical research and development.

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Required Skills

Regulatory Writing
Clinical Development
ICH Guidelines
FDA Regulations
EMA Regulations
Medical Documentation
Project Management
Scientific Writing
Review & Editing
Mentorship

About Clinical Careers Page

syneoshealth.com

Syneos 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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