Regulatory Publishing Specialist (eCTD )

Clinical Careers Page(1 month ago)

HybridFull TimeMedior$104,012 - $138,428 (estimated)Regulatory Affairs

About this role

A Regulatory Publishing Specialist (eCTD) at Syneos Health is a mid-level regulatory affairs role supporting the preparation and electronic publication of regulatory submissions for biopharmaceutical products. The position works within the clinical development organization to help ensure submission compliance with global regulatory standards and support timely dossier delivery to regulatory authorities.

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Required Skills

eCTD
Publishing
Quality Control
Assembler Tasks
Validation
Extedo eCTDManager
CoreDossier
Documentum
Acrobat
Microsoft Word

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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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