Urology Safety Program Manager

3 days ago


Minnetonka, Minnesota, United States Boston Scientific Full time

Safety Program Specialist Role

Senior Safety Program Specialist manages adverse event, device reporting, and safety deliverables for investigational and marketed products in the Urology division. The role involves overseeing project-specific safety plans, processing events and complaints, and acting as a key member of the clinical core team.

  • Author study-specific safety documents and plans to ensure compliance and execution.
  • Assess type/level of processing required for adverse events, ensuring timely and accurate completion.
  • Manage adverse event processing, including report review and safety query management to maintain high-quality data.
  • Ensure adjudication and reconciliation of safety events prior to data snapshots to prevent delays.
  • Provide critical input on safety-related matters to other study documents and processes.
  • Coordinate functional deliverables to meet study milestones, promoting efficient progress.
  • May perform medical review and assessment of adverse events in clinical trials, utilizing expertise in Urology therapeutic knowledge.

The ideal candidate will have 5 years of experience in clinical trials, with strong analytical and problem-solving skills. Additionally, they should possess in-depth knowledge of Urology therapeutic areas.

Boston Scientific is an equal opportunity employer and maintains a substance-free workplace. Compensation for this position is approximately $120,000 annually, reflecting the level of responsibility and expertise required.



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