[Hiring] Senior Risk Management Scientist @GE HEALTHCARE

Role Description

The Senior Risk Management Scientist provides scientific and operational support for global pharmacovigilance risk management and safety signal activities across the product lifecycle. The role supports the execution of risk management strategies, safety signal detection and evaluation, and regulatory compliance in line with global pharmacovigilance requirements. This position contributes to the development of Risk Management Plans, safety analytics, and governance deliverables, and supports preparation of materials and presentations for the Product Safety Review Board (PSRB). Reporting to the Head of Global Drug Safety and Risk Management, the role works cross‑functionally to ensure consistent, data‑driven risk oversight and effective safety communication.

Responsibilities

• Operational Leadership
  • Serve as an operational leader of the Drug Safety & Risk Management (DSRM) driving oversight, implementation, and tracking of all global PV risk management obligations, commitments, and risk minimization measures.
  • Coordinate and track reporting of safety issues to Product Safety Review Board (PSRB), Quality Management Review (QMR) and PV Leadership in compliance with internal procedures to ensure proper communication of risk is achieved and proper course of action is followed.
• Safety Signal Management & Safety Analytics
  • In collaboration with Sr Medical Director and statistician interpret safety data trends and ensure accurate integration of risk assessment into product labeling and RMPs.
  • Lead and coordinate bi-weekly Safety Review Team meeting and contributes to the preparation of a cross-functional Signal Investigation Meeting.
  • Lead the development of analytical tools, standard outputs, and data visualizations that support comprehensive signal evaluation.
  • Review Signal Detection outputs and notify Drug Safety & Risk Management (DS&RM) about safety observations of interest.
  • Serve as an Administrator in Veeva RIM for Safety Signal Workflow, UAT.
  • Coordinate and contribute to periodic ADR Trending review, works in collaboration with Medical Director.
  • Collect data and prepare monthly/ quarterly KPIs related to Safety Signals and ADR trending.
• Risk Management
  • Author/ lead development of Risk Management Plan(s) Development RMPs, and associated regulatory documents in accordance with Good Pharmacovigilance Practices and regional regulatory expectations.
• Cross-functional & Regulatory Collaboration
  • Work closely with cross-functional teams (e.g. Clinical Development, Medical Affairs, Regulatory Affairs) to ensure alignment of GEHCs global position for the PV risk management processes.
  • Work with Sr Risk Management Director, PV Physicians and PV Scientists on any Regulatory Submission/filing for MAA, etc. to be sure that risks are reflected properly and carried through to support filing activities.
• Aggregate Safety Reporting
  • Contribute to risk components of Aggregate reports like DSUR, PBRER and other periodic assessments, ensuring integration of current risk profiles and emerging safety data.
• Additional Responsibilities
  • Perform other duties related to the position as necessary and as defined in SOPs and/or at the request of supervisor.

Qualifications

• Advanced clinical degree (e.g., MD, DO, NP, PA, PharmD, PhD in a health-related field) required.
• Significant Experience of pharmaceutical/biotechnology PV experience, including clinical trial and post-marketing experience. Global experience preferred.
• Substantial Experience in PV / Safety.
• Strong knowledge in FDA, EU, ICH guidelines, initiatives and regulations governing pharmacovigilance.
• Strong knowledge in safety signal evaluation and responses to safety requests from Health Authorities.

Desired Skills

• Strong oral and written communication skills.
• Strong interpersonal and leadership skills.
• Demonstrated ability to analyze and resolve problems.
• Demonstrated ability to lead programs/projects.
• Ability to document, plan, market, and execute programs.
• Established project management skills.
• Strong track record of scientific and analytical thinking.

Behaviors

• Act with humility and build trust.
• Lead with transparency.
• Deliver with focus.
• Drive ownership – always with unyielding integrity.

Total Rewards

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.