Safety & PV Specialist I - Medical Device & PQC

Clinical Careers Page(7 days ago)

Gurugram, Haryana, IndiaOnsiteFull TimeJunior$41,343 - $56,343 (estimated)Pharmacovigilance

About this role

The Safety & Pharmacovigilance Specialist I at Syneos Health is responsible for managing safety data, processing adverse event reports, and ensuring compliance with global pharmacovigilance regulations. It involves handling product quality complaint cases and supporting safety reporting activities within clinical research and post-marketing safety programs.

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Required Skills

FDA
Regulatory Reporting
Argus
MedDRA
Pharmacovigilance
Safety Data Management
Clinical Trials
GCP
Reporting
Post-Marketing

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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