Senior Director, Clinical Pharmacology

Bristol Myers Squibb; Princeton (NJ); Presencial; USD 240 000 - 291 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Comprehensive benefits

Flexible time off

11 paid holidays

Resumo da oferta

Bristol Myers Squibb seeks a Senior Director of Clinical Pharmacology to provide scientific leadership across drug development programs in Princeton, NJ. You will guide PK/PD strategies and model‑informed drug development, mentoring CP&P leads and aligning plans with compound strategy.

You will influence study design, regulatory submissions, and cross‑functional collaboration while fostering a high‑performing team environment and ensuring rigorous data interpretation and reporting.

Qualificações

• MS, PhD or PharmD in relevant field or PharmD with post‑doctoral training.
• 10+ years’ experience in Clinical Pharmacology and Pharmacometrics.
• Deep knowledge of drug development and small molecule/biologic properties.
• Strong written and oral communication; team leadership.
• Ability to mentor CP&P staff; asset lead in development programs.
• Programming experience (NONMEM, R, WinNonlin, SAS) desirable.

Responsabilidades

• Mentor CP&P leads and oversee clinical pharmacology strategy across programs.
• Represent CP&P in cross‑functional disease strategy teams and governance forums.
• Contribute to Phase 2/3 design and registrational strategy.
• Oversee Clinical Pharmacology Plans and study design, data analysis and reporting.
• Drive portfolio strategy with senior leadership; collaborate with health authorities.

Conhecimentos

Clinical Pharmacology

Pharmacometrics

PK/PD

Model-Informed DDD

Leadership

Formação académica

MS/PhD/PharmD in relevant field

Ferramentas

NONMEM

R

WinNonlin

SAS

Descrição da oferta de emprego

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

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 https://careers.bms.com/benefits

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 https://careers.bms.com/ways-of-working.

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 [e-mail]. 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: https://careers.bms.com/california-residents/

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 https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.