Principal Clinical Trial Regulatory Affairs
Clinical Careers Page(21 hours ago)
About this role
Syneos Health is seeking a Principal Clinical Trial Regulatory Affairs professional to lead regulatory strategies for clinical trials within a global biopharmaceutical organization. The role involves working with cross-functional teams to ensure compliance with regulatory requirements and streamline approval processes.
Required Skills
- Regulatory Affairs
- Clinical Trials
- Regulatory Submissions
- GxP
- FDA
- EMA
- Pharmacovigilance
- Compliance
- Pharmaceuticals
About Clinical Careers Page
syneoshealth.comSyneos 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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