Director, Clinical Pharmacology and Pharmacometrics

About Bristol-Myers Squibb:

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support. 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 the resources to pursue their goals, both at work and in their personal lives.

This individual will apply their Clinical Pharmacology and Drug Development expertise to the development of small molecule and biologic assets in immunology that help patient prevail over serious autoimmune disease conditions. This individual will also provide broad clinical pharmacology and pharmacometrics strategic leadership to early and late stage assets. This person will play a central role in the planning, designing, executing, interpreting and reporting of healthy subject and patient studies conducted in early, full and life cycle stages of development. Provide critical input on the design and execution of Clinical Pharmacology plans and be able to create a robust human Clinical Pharmacology profile by integrating results from a broad spectrum of non-clinical, clinical and model-based assessments. In addition, this individual will be responsible for generating modeling and simulation plans, conducting population pharmacokinetic and exposure-response analyses for the assets, and managing analyses conducted by pharmacometrics vendors ensuring timely delivery of deliverables. This individual will serve as the Clinical Pharmacology subject matter expert on cross functional asset teams and provide his/her functional expertise during health authority interactions and regulatory submissions. Position requirements are as follows:

• Ph.D. in pharmaceutical sciences, biomedical engineering, or a PharmD with a clinical pharmacology research fellowship.
• A minimum of 7 years of experience gained through direct industry experience in Clinical Pharmacology is required.
• The successful applicant will have experience in developing clinical pharmacology plans and in the preparation of regulatory submissions (including INDs, NDAs, BLAs and/or significant sNDAs/sBLAs).
• This person will have experience in responding to regulatory questions related to all aspects of clinical pharmacology.
• This individual will have knowledge and experience in the application of current practices in the areas of clinical pharmacology, pharmacokinetics, drug metabolism, bioanalysis, biopharmaceutics, regulatory affairs, and toxicology.
• Strong oral and written communication skills necessary to formally present and report information internally and externally is required.
• The ability to work in a dynamic team oriented environment is essential.