Bristol-Myers Squibb

Associate Director, Patient Safety Scientist

Bristol-Myers Squibb

Princeton, NJ, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Welcome to Bristol-Myers Squibb, a leading global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines to patients in need. We are currently seeking a highly skilled and passionate Associate Director, Patient Safety Scientist to join our team. In this role, you will play a critical role in ensuring the safety and well-being of patients by overseeing the evaluation and management of adverse events and safety data for our products. If you are a driven and experienced professional with a background in pharmacovigilance and a strong dedication to patient safety, we encourage you to apply for this exciting opportunity.

  1. Oversee the evaluation and management of adverse events and safety data for our products.
  2. Ensure compliance with all pharmacovigilance regulations and guidelines.
  3. Collaborate with cross-functional teams to develop risk management plans.
  4. Monitor and analyze safety data to identify potential safety concerns.
  5. Conduct safety signal detection and evaluation.
  6. Communicate safety data and risk management plans to internal and external stakeholders.
  7. Provide guidance and support to team members on safety-related matters.
  8. Lead safety review meetings and provide recommendations for risk mitigation.
  9. Stay updated on industry trends and regulations related to patient safety.
  10. Develop and maintain relationships with key stakeholders, including regulatory agencies and healthcare professionals.
  11. Participate in the development and implementation of company-wide safety strategies.
  12. Assist in the preparation and submission of safety reports to regulatory agencies.
  13. Conduct training and education sessions on pharmacovigilance for internal teams.
  14. Collaborate with clinical development teams to ensure safety considerations are incorporated into clinical trial protocols.
  15. Act as a subject matter expert on patient safety for the company.
Where is this job?
This job is located at Princeton, NJ, USA
Job Qualifications
  • Advanced Degree In Life Sciences Or Related Field: A Minimum Of A Master's Degree In A Relevant Field Such As Pharmacovigilance, Epidemiology, Pharmacology, Or Public Health Is Typically Required For An Associate Director Role At Bristol-Myers Squibb. This Academic Background Provides A Strong Foundation For Understanding Scientific Principles And Applying Them To Patient Safety.

  • Minimum Of 5 Years Of Experience In Pharmacovigilance Or Drug Safety: Bristol-Myers Squibb Would Be Looking For Candidates With A Solid Foundation In Patient Safety And Experience Working In A Pharmaceutical Company Or In A Similar Role. This Experience Should Include A Deep Understanding Of Global Pharmacovigilance Regulations And Guidelines.

  • Knowledge Of Drug Development Process And Pharmacovigilance Practices: The Associate Director Should Have A Thorough Understanding Of The Drug Development Process And How Pharmacovigilance Fits Into It. They Should Also Have Experience With Safety Signal Detection, Risk Management, And Benefit-Risk Assessment.

  • Leadership And Project Management Skills: As An Associate Director, This Individual Would Be Expected To Lead A Team Of Patient Safety Scientists And Manage Projects Related To Safety Surveillance And Risk Management. They Should Have Excellent Communication, Organizational, And Interpersonal Skills To Effectively Lead Their Team And Collaborate With Cross-Functional Teams.

  • Regulatory Experience And Compliance Knowledge: Bristol-Myers Squibb Operates Globally And Is Subject To Various Regulatory Requirements. Candidates For The Associate Director Role Should Have Experience Interacting With Regulatory Agencies And Be Knowledgeable About Compliance Requirements Related To Pharmacovigilance. This Includes Knowledge Of Ich Guidelines, Gvp, And Other Relevant Regulations.

Required Skills
  • Risk Management

  • Data Analysis

  • Quality Management

  • Risk assessment

  • Regulatory compliance

  • Drug Safety

  • Pharmacovigilance

  • Safety Reporting

  • Safety Monitoring

  • Signal Detection

  • Adverse Events

Soft Skills
  • Communication

  • Conflict Resolution

  • Leadership

  • Time management

  • Interpersonal Skills

  • creativity

  • Teamwork

  • Adaptability

  • Problem-Solving

  • Empathy

Compensation

According to JobzMall, the average salary range for a Associate Director, Patient Safety Scientist in Princeton, NJ, USA is $120,000 - $150,000 per year. Salaries may vary depending on the specific company, experience level, and additional qualifications.

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 PostedJune 26th, 2025
Apply BeforeOctober 28th, 2025
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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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