Director, Pharmacovigilance Scientist

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Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits services and programs that provide our employees with the resources to pursue their goals both at work and in their personal lives. Read more: Summary

The Director Patient Safety Scientist is a key partner and strategic advisor to Medical Safety Assessment Physician (MSAP)/Safety Management Team (SMT) Chair to characterize conditions for safe use of BMS medicines and proactively communicate safety evidence to influence decision-making for assets in development and marketed products by evaluating and mitigating risks. Independently performs core signal detection activities and elevates program or portfolio issues impacting key SMT programs priorities resources and milestones. Leads safety data review meetings (SDRMs). Ensures pharmacovigilance regulatory compliance.

Position Responsibilities

Signal Detection/Management & Safety Surveillance:

• Develops or co-develops the global safety strategy in partnership with the SMT Chair overseeing signal detection and assessment across the product lifecycle for multiple complex compounds. Utilizes advanced tools and diverse data sources to investigate safety concerns enabling proactive risk management and informed decision-making.

• Leads execution for signal evaluation (e.g. case-series literature review health authority/claims databases) promotes cross-functional collaboration with authors for comprehensive signal reports develops clear preliminary conclusions and ensures timely tracking stakeholder engagement and documentation within the signal management system.

• Develops strategy and provides strong medical writing for safety and risk management sections of aggregate safety documents (eg DSUR PBRER PADER).

• Develops strategy analyzes data and writes ad hoc responses to health authorities (including supporting local markets in responding to risk management-related queries from local HAs) and mentors less experienced scientists in this area.

Clinical Development Product Support:

• Leads the preparation review and strategic input for safety sections in key clinical trial documents such as protocols clinical study reports (CSR) investigator brochures (IB) including reference safety information (RSI) informed consent forms (ICF) and contraception language.

• Represents Patient Safety and supports safety strategy preparation at internal and external meetings (pre-submission Advisory Committees Scientific Advice data monitoring committee publications etc.).

Submission Planning & Postmarketing Product Support:

• In partnership with the SMT Chair co-develops safety strategy and input for regulatory filings including the formulation of safety strategy key safety messages and risk management approaches. Provides expert oversight and authorship of safety sections on marketing authorization applications (MAA) including safety table shells Integrated Summary of Safety (ISS) Summary of Clinical Safety (SCS) clinical overview briefing documents and initial product labeling (USPI CCDS SmPC). Leads cross-functional responses to ad hoc regulatory safety requests (eg 120-day safety updates) proactively sourcing and interpreting safety data to evaluate the impact of emerging safety issues on the products benefit-risk profile.

• Provides expert analysis and strategic input analyzes data and authors documentation as needed to support safety labeling updates to adequately reflect emerging postmarketing safety profile.

• Supports the EU QPPV or other regional/local QP for safety issues on assigned products.

Risk Management Planning & Execution:

• Creates strategy for creation and update of the EDSR to proactively characterize emerging safety concerns during asset development support Structured Benefit Risk and define the strategy for Company Core Risk Management and gaining alignment with SMT/governance including collaboration with Epidemiology on risk minimization effectiveness non-interventional research (NIR) activities for post-authorization safety studies (PASS).

• Provides strategic leadership and is accountable for the development and maintenance of global and EU Risk Management Plans (RMPs) including understanding of in-licensing arrangements or pharmacovigilance agreements that may impact risk management activities.

• Leads and oversees the creation and revisions to core additional Risk Minimization Measures (aRMMs) and additional Pharmacovigilance Activities (aPVAs) globally and locally. Provides guidance to local markets and vendors for complex (eg Pregnancy Prevention Programs Controlled Distribution Programs) and non-complex aRMMs (eg educational materials).

Department Activities:

• Oversees a global team of safety scientists and risk management experts within the assigned therapeutic area.

• Leverages automation and innovation tools into day-to-day work. Drives digital change initiatives including management of stakeholder expectations and overcoming resistance. Uses multiple data sources and AI generated outputs to support decisions.

• Supports preparation for regulatory inspections and audits as a subject matter expert through proactive evaluation of current processes; assesses alignment with regulatory expectations guidelines and mandates.

• Fosters a high-performing and collaborative safety team by actively engaging with all TA staff serving as a strategic partner and role model in cross-functional interactions and promoting a culture of excellence accountability and continuous improvement.

Cross Functional Activities:

• Leads or identifies opportunities for process improvements and cross-functional initiatives for Patient Safety Science including update and maintenance of procedural documents.

• Builds cross-functional partnerships with SMT/ACT stakeholders exercising strong matrix leadership to drive alignment accountability and timely decision-making across functions.

• Possesses deep knowledge of product goals strategy drug development milestones partnership agreements HA commitments functional area responsibilities and relevant global HA regulations and industry trends; shares with cross-functional teams as needed.

Degree & Experience Requirements

• Scientific degree (e.g. BS MS RN PharmD PhD MD) or other degree with the equivalent combination of relevant education and professional experience

• Minimum of 8 years relevant pharmacovigilance/pharmaceutical industry/drug development experience; demonstrated ability to mentor and coach others

Key Competency Requirements

• Demonstrated ability to develop and execute safety strategy across complex cross-functional initiatives in drug development pharmacovigilance and global regulatory safety.

• Deep scientific and medical expertise with the ability to synthesize complex data (clinical nonclinical postmarketing literature) to inform strategic decisions and influence stakeholders.

• Strong decision-making skills grounded in scientific rigor sound judgment and experience.

• Effective matrix leader with strong organizational facilitation and communication skills to drive alignment and engagement across internal and external networks and senior leaders.

• Highly adaptable and resilient in dynamic environments; consistently demonstrates initiative and professionalism.

• Ability to incorporate emerging technologies (including AI automation tools and digital platforms) to streamline workflows enhance data analysis and reduce manual effort while maintaining scientific rigor and compliance with safety standards.

If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job such as required skills where the job is performed the employees work schedule job-related knowledge and experience. Final individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits please visit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

• Health Coverage: Medical pharmacy dental and vision care.

• Wellbeing Support: Programs such as BMS Well-Being Account BMS Living Life Better and Employee Assistance Programs (EAP).

• Financial Well-being and Protection: 401(k) plan short- and long-term disability life insurance accident insurance supplemental health insurance business travel protection personal liability protection identity theft benefit legal support and survivor support.

Work-life benefits include:

Paid Time Off

• US Exempt Employees: flexible time off (unlimited with manager approval 11 paid national holidays (not applicable to employees in Phoenix AZ Puerto Rico or Rayzebio employees)

• Phoenix AZ Puerto Rico and Rayzebio Exempt Non-Exempt Hourly Employees: 160 hours annual paid vacation for new hires with manager approval 11 national holidays and 3 optional holidays

Based on eligibility* additional time off for employees may include unlimited paid sick time up to 2 paid volunteer days per year summer hours flexibility leaves of absence for medical personal parental caregiver bereavement and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours depending on the nature of their work and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors leased workers and other service providers are not eligible to participate in the program.

Uniquely Interesting Work Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

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