Principal Clinical Trial Regulatory Affairs - +4 years of experience in regulatory submissions in LATAM - Home Based

Clinical Careers Page(3 days ago)

RemoteFull TimeSenior$85,000 - $120,000Regulatory Affairs

About this role

A Principal Clinical Trial Regulatory Affairs professional at Syneos Health provides expertise in regulatory submissions for clinical trials, managing strategic relationships with clients, leading regulatory activities, and ensuring compliance with applicable laws and guidelines. This role supports the development and maintenance of clinical trial documentation and oversees regulatory processes within clinical research projects.

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Required Skills

Regulatory Affairs
Clinical Trials
Regulatory Submissions
GxP
GCP
ISO 14155
Budgeting
Quality Management
Medical Device
Risk Assessment

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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