Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; US/CAN
Clinical Careers Page
About this role
A Senior or Principal Medical Writer specializing in regulatory documentation at Syneos Health focuses on producing clear, accurate, and compliant medical writing deliverables for clinical development projects. The role involves managing complex documentation processes, coordinating with various departments, and ensuring regulatory standards are met to facilitate drug submissions and approvals.
Skills
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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About Clinical Careers Page
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Leadership Team
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
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and employee contacts for Clinical Careers Page.
Salary
$81k – $145k
per year