Associate Director, Clinical Pharmacology

Working with Us Challenging. 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. Position Summary The Associate Director, Clinical Pharmacology drives the implementation, planning, and execution of clinical pharmacology activities across assigned projects, operating with a high degree of independence while partnering collaboratively within the function. In this role, the Associate Director leads trial-level activities and supports the development of compounds across relevant therapeutic areas, applying strong Pharmacokinetics/Pharmacodynamics (PK/PD) principles and model-based analyses to inform and advance drug development decisions. The Associate Director works cross-functionally to contribute to and help shape functional development strategies, while also serving as a mentor within the Clinical Pharmacology and Pharmacometrics organization to support the continued growth and development of the team. Key Responsibilities: * Independently contribute to the development of compounds across various therapeutic areas with some supervision * Provide input to Phase 2/3 clinical study design and registrational strategy design for the compound with supervision * 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; serves as Clinical Pharmacology subject matter expert * Lead or participate in departmental initiatives; may be involved in external initiatives based on proficiency * Provide expertise based on proficiency to Business Development teams Qualifications & Experience: * MS, PhD or PharmD in relevant field * 5+ years’ experience with demonstrated progression in Clinical Pharmacology and Pharmacometrics knowledge, including experience with general drug development process and 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 * Provide mentorship and guidance to staff and the CP&P function * Supervise a colleague in CP&P, as needed * Independently serve as the CP&P lead for one or more assets in the BMS drug development program * 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 If 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. Compensation Overview: Cambridge...