Head of USCAN, Pharmacovigilance
Summary
The Head of Pharmacovigilance at GE HealthCare will lead and oversee all USCAN pharmacovigilance activities to ensure the safety of the company's products. This is a senior leadership role, and although an individual contributor position, it is mission critical for the company with responsibilities that encompasses strategic planning, implementation, and management of pharmacovigilance systems and processes in compliance with regulatory requirements.
- Be the expert and face of Drug Safety and PV in the US market
- Develop and implement pharmacovigilance strategies and systems
- Oversees domestic ICSRs and is responsible for overall quality of ICSR submissions
- Ensure compliance with global regulatory requirements and guidelines
- Rigorously ensure the collection, analysis, and reporting of adverse event data to the highest GEHC standards
- Collaborate with cross-functional teams, including commercial, medical, clinical, regulatory, and quality assurance
- Monitor and evaluate the safety profile of the company's products
- Stay updated on changes in pharmacovigilance regulations and guidelines
- Day-to-day responsibilities, including but not limited to: PV training activities, medical review, medical writing, perform PV awareness and educational sessions
- Informal leadership (matrix organization of consisting of case processing/distribution, customer-facing functions in other organizations, aggregate reports, clinical trial safety for studies in USCAN, responses to questions from FDA)
- Supervises follow-up with reporters
- Support PV inspections, audits and health authority queries
- Communicates with internal stakeholders, customers, as needed
- Review and medically assess Individual Case Safety Reports (ICSRs) , including serious and unexpected adverse events.
- Support Risk Evaluation and Mitigation Strategies (REMS) and Periodic Benefit-Risk Evaluation Reports (PBRERs) .
- Responsible for quality of responses to safety questions from local health authorities
- Additional responsibilities as directed by Global Head of PV&DS
- Participate in global signal detection , risk management planning , and aggregate report preparation (e.g., DSURs, PSURs).
- Provide medical input into global safety governance meetings , including Safety Review Teams and Risk Management Committees.
- Collaborate with EU QPPV and regional safety leads to ensure harmonized safety strategies across geographies.
- MD or equivalent medical degree required;
- 10+ years in Pharmacovigilance, Medical Affairs and/or Regulatory Affairs in a Pharmaceutical company or CRO, (with at least 10 years in Pharmacovigilance) at local, regional or global levels, and ideally several, with direct USCAN experience
- Excellent communication and interpersonal relationship skills, proven analytical skills, proven proficiency with office packages, demonstrable experience with Chatbots (ChatGPT, Copilot, Claude, Perplexity, etc.) and global safety data base experience (e.g. Argus)
- Willingness to travel within USCAN (30%)
- Strong knowledge of global pharmacovigilance regulations and guidelines, especially US FDA
- Ability to work effectively in a cross-functional team environment
- Experience in a leadership role within a pharmaceutical or biotechnology company
- Experience with regulatory PV inspections and interactions with regulatory authorities
- Certification in pharmacovigilance or drug safety
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