About the job
Pharmacovigilance Scientist – EU/UK Based (Remote)
Location: Remote (EU/UK)
Type: Full-time | Freelance/Contract Options Considered
We’re currently partnered with a leading pharmacovigilance services and technology provider seeking a Pharmacovigilance (PV) Scientist to join their growing global team. This company is known for delivering smart, scalable drug safety solutions powered by deep domain expertise and innovative technologies — supporting clients across the entire pharmacovigilance life cycle.
About the Role:
As a PV Scientist, you’ll work closely with Safety Physicians and Global Safety Officers to support the detection, assessment, and prevention of adverse effects, contributing to regulatory submissions and benefit-risk evaluations across multiple projects.
Key Responsibilities:
- Support benefit-risk evaluations and safety decisions with cross-functional safety teams
- Assess adverse events (AEs) and safety data from clinical trials
- Assist in developing safety narratives and summaries for regulatory submissions
- Contribute to signal detection and safety signal management
- Prepare and review safety documents including PSURs, PBRERs, DSURs, and RMPs
- Stay up to date on evolving global PV regulations and best practices
- Contribute to SOP/WI development and inspection readiness activities
Ideal Background:
- Degree in life sciences, pharmacy, medicine, or related field
- 3–5 years of PV experience, ideally in safety science or risk management
- Strong knowledge of AE management and clinical trial processes
- Experience with regulatory submissions and working with global safety teams
- Detail-oriented with excellent analytical and communication skills
Preferred Skills:
- Familiarity with safety databases (e.g., Argus, ArisG, Veeva Vault Safety)
- Fluent in English (spoken and written); additional languages a plus
- Proficient in Microsoft Office tools