Bristol-Myers Squibb

Executive Director, Head of Pharmacovigilance - Safety Science

Bristol-Myers Squibb

San Diego, CA, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Are you a highly experienced and driven leader with a passion for ensuring patient safety in the pharmaceutical industry? Do you possess a strong background in Pharmacovigilance and a track record of successfully managing Safety Science teams? If so, Bristol-Myers Squibb has an exciting opportunity for you as our Executive Director, Head of Pharmacovigilance - Safety Science. Join our dynamic and innovative team and make a meaningful impact on the lives of patients worldwide. We are seeking a visionary and strategic leader to drive our global safety efforts and ensure compliance with regulatory requirements. The ideal candidate will have a minimum of 10 years' experience in senior-level Pharmacovigilance roles, a deep understanding of international regulations, and a proven ability to lead and develop high-performing teams. If you are ready to take on a challenging and rewarding leadership role, we encourage you to apply today.

  1. Develop and implement global safety strategies and policies in alignment with regulatory requirements and company objectives.
  2. Lead and manage the Safety Science team, providing direction, guidance, and support to ensure the delivery of high-quality and timely safety data and reports.
  3. Oversee the pharmacovigilance activities of the company, including signal detection, risk management, and safety monitoring.
  4. Ensure compliance with international regulations and guidelines related to pharmacovigilance and patient safety.
  5. Collaborate with cross-functional teams and external partners to support the development, submission, and maintenance of drug safety information.
  6. Maintain a deep understanding of the evolving pharmacovigilance landscape and proactively identify opportunities for improvement and innovation within the organization.
  7. Build and maintain strong relationships with key stakeholders, including regulatory agencies, to ensure effective communication and collaboration.
  8. Provide strategic input and support for product development and lifecycle management activities, including risk-benefit assessments and benefit-risk management plans.
  9. Participate in industry forums and conferences to stay informed of industry best practices and trends.
  10. Mentor and develop team members to promote a culture of continuous learning and growth within the organization.
  11. Represent the company in interactions with external parties, including regulatory authorities, industry groups, and vendors.
  12. Report to senior management on the performance of the pharmacovigilance function and provide strategic recommendations for improvement.
  13. Ensure the timely and accurate submission of all required safety reports to regulatory authorities.
  14. Foster a culture of patient-centricity and safety awareness throughout the organization.
  15. Collaborate with other functional areas, such as clinical development and medical affairs, to ensure a holistic approach to patient safety.
  16. Manage the budget and resources for the Pharmacovigilance - Safety Science team.
  17. Stay updated on industry trends and regulations related to pharmacovigilance and incorporate them into company processes and procedures.
  18. Ensure that all pharmacovigilance activities are conducted in accordance
Where is this job?
This job is located at San Diego, CA, USA
Job Qualifications
  • Extensive Knowledge And Experience In Pharmacovigilance And Safety Science, Including A Strong Understanding Of Global Regulations And Guidelines.

  • Proven Leadership Skills With A Minimum Of 10 Years Of Experience In A Senior Pharmacovigilance Role.

  • Excellent Communication And Project Management Abilities, With The Ability To Effectively Collaborate With Cross-Functional Teams.

  • Experience In Managing And Developing A Team, Including Setting Strategic Goals And Providing Mentorship And Guidance.

  • Advanced Degree In A Relevant Field Such As Pharmacy, Medicine, Or Life Sciences, With A Strong Track Record Of Continuous Learning And Professional Development.

Required Skills
  • Strategic Planning

  • Project Management

  • Data Analysis

  • Communication

  • Team Management

  • Problem Solving

  • Leadership

  • Risk assessment

  • Drug Safety

  • Pharmaceutical Industry Knowledge

  • Pharmacovigilance Regulations

Soft Skills
  • Communication

  • Conflict Resolution

  • Emotional Intelligence

  • Leadership

  • Time management

  • creativity

  • Attention to detail

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Executive Director, Head of Pharmacovigilance - Safety Science in San Diego, CA, USA is $200,000-$240,000 per year. However, this can vary depending on the specific company, level of experience, and other factors. It is always best to research the specific company and job listing to get a more accurate salary range.

Additional Information
Bristol-Myers Squibb is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedFebruary 25th, 2025
Apply BeforeJune 9th, 2026
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About Bristol-Myers Squibb

Bristol-Myers Squibb Co. operates as a biopharmaceutical company, which engages in the discovery, development, licensing, manufacturing, marketing, distribution, and sale of biopharmaceutical products. It includes chemically-synthesized drugs or small molecules and products produced from biological processes called biologics.

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