Safety & PV Submission Specialist I (Clinical Trial + Regulatory Intelligence) - ARG Office Based

Clinical Careers Page(22 days ago)

Buenos Aires, ArgentinaOnsiteFull TimeJunior$68,469 - $91,834 (estimated)Clinical Development

About this role

A Safety & PV Submission Specialist I at Syneos Health supports safety reporting activities within clinical trials, ensuring compliance with global regulations and maintaining safety documentation. The role involves collaboration with project teams, regulatory intelligence, and data management to facilitate timely safety submissions.

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Required Skills

Safety Reporting
Pharmacovigilance
Regulatory Intelligence
GCP
ICH Guidelines
Documentation
Safety Submissions
Clinical Trials
Regulatory Compliance
Data Management

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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