An innovative biopharmaceutical organisation is seeking an experienced Associate Director within Safety Surveillance and Aggregate Reporting to provide scientific and strategic leadership across global pharmacovigilance activities.

Key Responsibilities

• Lead safety surveillance activities for assigned products.
• Oversee signal detection and risk management activities.
• Author/review aggregate safety reports including DSURs, PBRERs, and PADERs.
• Lead development of EU and core Risk Management Plans (RMPs).
• Support safety sections for global regulatory submissions (NDA/MAA).
• Manage clinical and post-marketing safety activities.
• Ensure compliance with global pharmacovigilance regulations.
• Collaborate cross-functionally and mentor junior team members.

Requirements

• Degree in Life Sciences or related field; advanced degree preferred.
• Extensive pharmacovigilance experience withi...