Senior Director, Clinical Pharmacology

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Position Summary The Senior Director, Clinical Pharmacology provides strategic and scientific leadership for clinical pharmacology activities across drug development programs. This role leads the planning and execution of clinical pharmacology strategies, including PK/PD and model-informed drug development approaches, and oversees development and delivery of Clinical Pharmacology & Pharmacometrics plans aligned with compound strategy. The Senior Director serves as a key member of Clinical Pharmacology leadership and cross-functional program teams, influencing development strategy and decision-making while fostering a collaborative, high-performing learning environment. Key Responsibilities

• Manage and mentor other CP&P leads as appropriate
• Responsible and accountable for clinical pharmacology strategy across all phases of development
• Represent the ClinPharm department on cross-functional disease strategy teams and on relevant governance forums
• Provide input to Phase 2/3 clinical study design and registrational strategy
• Supervise the development of the Clinical Pharmacology Plan(s)
• Supervise design of Clinical Pharmacology studies and manages data analysis, interpretation, and reporting
• Drive decision-making and strategy over the entire portfolio or critical portions of the portfolio of compounds, through effective partnership with senior leaders
• High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses
• Lead collaboration on cross-functional drug development teams, regulatory submissions, and departmental initiatives; serves as Clinical Pharmacology subject matter expert
• Represent department in interactions with health authorities; serve as Clinical Pharmacology subject matter expert
• Oversee internal initiatives and serves as department representative on external initiatives
• Work with Business Development teams and provide critical expertise to assess external acquisitions
• Responsible for administrative deliverables such as creating Therapeutic area level departmental objectives, hiring / retaining talent, maintaining budgets, etc.

Qualifications & Experience

• MS, PhD or PharmD in relevant field or a PharmD with post-doctoral training
• Approximately 10+ years’ experience with demonstrated progression in Clinical Pharmacology and Pharmacometrics, including extensive expertise in the general drug development process and in small molecule and/or biologic drug property characterization
• In-depth knowledge of current practices and issues in Clinical Pharmacology and Pharmacometrics
• Strong written and oral communication skills necessary to report on and deliver scientific presentations
• Demonstrated ability to work in a dynamic team-oriented environment
• Manage a team of CP&P scientists and provide mentorship and guidance to staff and CP&P function
• Independently serve as the CP&P lead for one or more assets in the BMS drug development program
• Demonstrated leadership abilities, expanded sphere of influence, and stakeholder management in a matrix environment
• Programming experience is highly desired (e.g., NONMEM, R, and WinNonlin. SAS, Splus, etc.)
• Quantitative data analysis, POP PK/PD, and data visualization skills are highly desired

#LI-Hybrid We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. Compensation Overview: Princeton - NJ - US: $239,860 - $290,656 The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance. Benefits: Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability). U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year. Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays. Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day. U.S.-based job seekers can explore full benefit offerings at How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at [ 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 [View email address on us.fitly.work](mailto:View email address on us.fitly.work). Visit [careers.bms.com/eeo-accessibility]( to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: [ For roles based in Washington state only: If you live in or expect to work from Washington State if hired for this position, please visit [this page]( for important information about the Washington Fair Chance Act. Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at [ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [View email address on us.fitly.work](mailto:View email address on us.fitly.work)with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account. R1607830 : Senior Director, Clinical Pharmacology