Regulatory Publishing Specialist- Veeva Experience Required

Clinical Careers Page(1 month ago)

HybridFull TimeSenior$124,981 - $168,503 (estimated)Regulatory Affairs

About this role

A Regulatory Publishing Specialist at Syneos Health supports the preparation and delivery of regulatory submission documentation for biopharmaceutical clients, ensuring adherence to global submission standards and quality expectations. The role operates within the clinical development organization and collaborates with cross-functional teams and document authors to facilitate timely regulatory filings.

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Required Skills

Veeva Vault
eCTD
Publishing
Submission Assembly
Quality Control
PDF Formatting
Word Formatting
Document Management
Troubleshooting
Team Leadership

+1 more

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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