Syneos Health
A Regulatory Consultant at Syneos Health leverages a background in life sciences to independently manage regulatory submissions, gap analyses, and lifecycle management for pharmaceutical clients. The role requires expertise in CMC modules and EU/GCC markets, involving collaboration across multidisciplinary teams to support product development and compliance. Consultants also prepare briefing packages, manage project timelines, and ensure adherence to global regulatory policies while contributing to business development efforts.
Headquarters
Morrisville, North Carolina, United States
Company Size
10001+ employees
Founded
2017
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.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
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
View leadership team, funding history,
and employee contacts for Syneos Health.
Syneos Health didn’t post a salary, so this is our estimate from similar listings.
32% below the average for this role
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