Clinical Trial Regulatory Specialist

Clinical Careers Page(5 days ago)

Belgrade, SerbiaOnsiteFull TimeMedior$40,000 - $60,000Regulatory Affairs

About this role

The Clinical Trial Regulatory Specialist supports regulatory activities in clinical trial documentation and submissions, ensuring compliance with applicable regulations and quality standards. They collaborate with the team to prepare and review core documentation required for site initiation and regulatory approvals within a global biopharmaceutical context.

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Required Skills

GxP
Regulatory Submissions
Quality Control
Documentation
EU Regulations
Clinical Trials
Microsoft Office
Agency Interactions
Risk Management
GCP

Qualifications

BA or BS in a related field
Experience with GxPs

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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