Associate Director, Structured Benefit-Risk Assessment Lead

Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.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: careers.bms.com/working-with-us.About the RoleWe're looking for an experienced SBRA Lead to drive structured benefit-risk assessments across BMS's portfolio — from early clinical development through to post-marketing. Reporting to the Head of SBRA within Safety Evidence & Sciences, you'll be the go-to expert for benefit-risk methodology, leading cross-functional teams and shaping company-wide positions on the benefit-risk profiles of our medicines.This role sits at the heart of cross-functional collaboration, working closely with medical safety assessment, clinical development, global regulatory, epidemiology, and beyond to deliver robust, well-evidenced benefit-risk positions.Directly reporting to: Head of Structured Benefit-Risk AssessmentWhat You'll DoProduct Scientific LeadershipLead end-to-end benefit-risk assessments across all therapeutic areas, from early clinical development through late-stage and post-marketingGuide, steer, and mentor cross-functional Benefit-Risk Project Teams (BRPTs) in the application of structured benefit-risk assessment frameworks, value trees, effects tables, and other relevant toolsOwn the development of the Core SBRA document and facilitate effective communication and collaboration among internal stakeholders to achieve consensus on the benefit-risk profile of BMS medicinesDrive strategic discussions on the use of qualitative and/or quantitative methods for benefit-risk assessmentChampion the patient voice by providing guidance on the incorporation of patient preference studies and patient-focused drug development into the assessment processServe as subject matter expert for the BRPT and wider functions on SBRA content, methodology, tools, and processesContinuously improve standard benefit-risk tools and frameworks in line with evolving best practicesStrategic Planning & OversightSupport the Head of SBRA in defining and executing the strategic vision for the benefit-risk assessment function, aligned with organizational goals and regulatory requirementsMonitor the regulatory landscape to ensure compliance and adoption of best practices, keeping up to date with guidance from regulatory agencies and key industry organizationsDevelop and maintain procedural documents and internal training materials related to benefit-risk assessment processesBuild and maintain relationships with internal partners and external thought leaders in the benefit-risk fieldCommunicate and innovate — develop novel ways to present benefit-risk information, author publications, and represent BMS at internal and external meetings and conferencesWhat You'll BringQualificationsBS/BA required; advanced degree strongly preferred (MSc, PhD, PharmD or equivalent)10+ years of relevant pharmaceutical, clinical, academic, or healthcare industry experience, with significant expertise in global pharmacovigilance, safety risk management, and benefit-risk assessmentStrong knowledge of global regulatory frameworks and processes for pharmacovigilance and benefit-risk managementProven track record of delivering against complex programmes within a highly matrixed organizationSkills & AbilitiesExemplary leadership skills with a proven ability to foster partnerships both within and across organizational boundariesStrong analytical mindset with creative problem-solving abilities — including in challenging and ambiguous situationsExceptional listening, communication, and stakeholder management skillsSkilled at managing multiple priorities, adapting to shifting demands, and operating effectively under uncertaintyAbility to handle conflict constructively, read situations quickly, and find common ground to drive resolutionUp to 5–10% travel required#LI-HybridIf you come across a role that intrigues you but doesn’t 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.Uniquely Interesting Work, Life-changing CareersWith 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 ProtocolBMS 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-bas