Be the expert behind safer medicines-leading signal detection and global safety strategy.

Proclinical is seeking a Senior Pharmacovigilance Specialist to support safety management activities for pharmaceutical products in the cardiovascular space. In this role, you will lead critical pharmacovigilance processes, including safety signal management, aggregate report preparation, and regulatory responses. You will also act as a subject matter expert on global safety regulations and guidelines, ensuring compliance and maintaining product integrity throughout clinical trials and post‑marketing phases.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities

• Lead safety signal management processes, including detection, tracking, documentation, and evaluation of safety data.
• Synthesize data from multiple sources and author signal evaluation reports.