Senior Safety Scientist / Associate Director / Director

Safety Science and Pharmacovigilance Role

Roche is seeking a professional to join our safety team to deliver knowledge on medicine safety profiles, manage patient risks, and coordinate pharmacovigilance activities. This role involves providing safety science support across the Roche portfolio, from early development through post-market stages.

Responsibilities

• Provide safety oversight and input into study management and clinical development strategy.
• Lead post-market safety activities, including signal evaluation, benefit-risk assessment, and risk management.
• Manage individual and aggregate case reporting, including ICSR, DSUR, and PBRER.
• Drive signal detection and contribute to the strategic review of safety assessments.
• Prepare and maintain labeling documents, risk communications, RMP, and REMS.
• Act independently to pursue professional development and manage safety responsibilities.

Requirements

• Postgraduate qualification in Life Sciences, Medicine, or Pharmacy is advantageous.
• Strong understanding of GxP, regulated processes, and the clinical trial lifecycle.
• Excellent written and verbal communication skills for global collaboration.
• Proficiency in complex data analysis and statistical methods for scientific data interpretation.
• Strong presentation skills for summarizing key considerations to diverse audiences.
• Proven ability to work independently with minimal supervision.