Principal Medical Writer - Regulatory Submission Documents

Clinical Careers Page(2 months ago)

HybridFull TimeSenior$80,600 - $145,000Medical Writing

About this role

A senior scientific writing role at Syneos Health focused on producing high-quality regulatory submission and clinical development documents for biopharmaceutical programs. The position operates within the clinical development organization and interfaces with cross-functional teams and clients to support regulatory submissions and documentation standards. It represents a subject-matter expert in regulatory and scientific communications for drug development.

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Required Skills

Medical Writing
Regulatory Guidelines
Clinical Research
Project Management
Editing
Proofreading
Literature Search
MS Office
Mentoring
Communication

Qualifications

Bachelor's Degree
Graduate Degree Preferred

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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