Director, Clinical Pharmacology

Position Summary

The Director, Clinical Pharmacology is responsible for leading the planning, implementation, and execution of clinical pharmacology strategies across one or more development programs, reporting to the Senior Director, Clinical Pharmacology & Pharmacometrics.

This role drives trial- and program-level activities, applying pharmacokinetics/pharmacodynamics (PK/PD) principles and model-informed approaches to support decision-making throughout drug development.

The Director partners cross-functionally to shape and deliver integrated development strategies, contributes as a key member of Clinical Pharmacology leadership and program teams, and ensures the development and execution of robust Clinical Pharmacology & Pharmacometrics (CP&P) plans aligned with compound strategy.

In addition, the role fosters a collaborative and supportive environment that promotes scientific excellence and continuous learning.

Key Responsibilities

Supervise and/or mentor other CP&P leads as appropriate Independently contribute to compound development across various development phases Represent Clinical Pharmacology at asset teams at governance based on proficiency Provide input to Phase 2/3 clinical study design and registrational strategy Accountable for Clinical Pharmacology and Pharmacometrics Plan Lead design of Clinical Pharmacology studies and manages data analysis, interpretation, and reporting High proficiency in PK, PK/PD, and model informed drug development (MIDD) principles and analyses Collaborate on cross-functional drug development teams, regulatory submissions, and departmental initiatives; serves as Clinical Pharmacology subject matter expert Participate in interactions with health authorities; serve as Clinical Pharmacology subject matter expert Lead and participate in departmental initiatives and represent CP&P on cross-functional initiatives / workstreams / taskforces Work with Business Development teams and provide critical expertise to assess external acquisitions Qualifications & Experience: MS, PhD or PharmD in relevant field or a PharmD with clinical pharmacology research fellowship Approximately 7+ years' experience with demonstrated progression in Clinical Pharmacology and Pharmacometrics, including 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 Demonstrate the ability to work in a dynamic team-oriented environment Manage 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 stakeholder management with strong influence/leadership 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: $201,910 - $244,666 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.

• 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.
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• R1606954: Director, Clinical Pharmacology