Regulatory Specialist - Germany

Clinical Careers Page(6 days ago)

OnsiteFull TimeMedior$75,000 - $95,000Regulatory Affairs

About this role

The Regulatory Specialist at Syneos Health in Germany supports clinical trial start-up activities, ensuring regulatory compliance and efficient project execution. The role involves collaboration with multiple functional areas and oversight of regulatory submissions and documentation to facilitate successful clinical studies.

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Required Skills

Regulatory Submissions
Clinical Trials
Project Management
BioPharmaceutical
Regulatory Strategy
Documentation
Quality Assurance
Communication
Timeline Management
Amendments

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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