Bristol Myers Squibb
Senior Director, Immunology and Neuroscience, Medical Evidence Generation
Bristol Myers Squibb, Madison, New Jersey, us, 07940
Senior Director, Immunology and Neuroscience, Medical Evidence Generation
Senior Director, Immunology & Neuroscience (I&N), Medical Evidence Generation (MEG) role in Global Medical Affairs manages the evidence generation for the I&N portfolio (including Medical Affairs Sponsored studies [MAST], Clinical Research Collaborations [CRC], and investigator-sponsored studies [ISR]) and provides leadership for the cross-functional teams executing on the book of work. The I&N MEG Senior Director leads cross-functional matrix teams to build relationships and source research concepts addressing critical evidence gaps for assets in prioritized indications. The Senior Director reports to the Immunology & Neuroscience Executive Director. Responsibilities include: Build, manage, and coach a sustained high-performance, externally focused global team accountable for defining and executing the I&N portfolio to address key data gaps Coach a team of MEG Leads, including Clinical Scientists and Clinical Trial Physicians, in oversight of Medical clinical trials end-to-end (start-up, governance, contract negotiation and execution, oversight, and readout support) Design and drive strategies to identify and advance new medical trials that accelerate the development of the BMS pipeline Demonstrate experience in clinical concept development and partnering across the drug development continuum Lead cross-functional teams on scientific and study-related activities to ensure robust results Contribute to the evolution of the MEG organizational model and operational infrastructure Accountable for the I&N MEG book of work (MASTs, ISRs, CRCs, IEP development) ensuring alignment with the Integrated Evidence Plan (IEP) and timely, rigorous execution Oversee medical study protocol and ICF development with input to ensure clinical relevance, scientific rigor, patient safety, and alignment with study objectives Maintain scientific integrity and data quality during trial execution across all phases Co-develop and maintain IEPs with Medical, HEOR, Development and other stakeholders Partner with Medical Affairs and Drug Development to ensure cohesiveness and a single MEG voice Apply business acumen and fiscal stewardship to drive scientific value and allocate resources per company priorities Assist in concept reviews through the RFP process, providing context for ongoing work, areas of interest, and upcoming readouts Qualifications & Experience MD preferred (or international equivalent) 5+ years of clinical trial experience in the pharmaceutical industry (e.g., Clinical Trial Physician, Clinical Scientist); proficiency in drug development and managing company-sponsored trials and leading teams 5+ years of strategic leadership experience in pharma, with understanding of clinical and business development, Medical Affairs, and related functions 10+ years of experience in clinical science or clinical research Strong communication, leadership, and collaboration skills; ability to influence decisions at all levels Experience building and leading high-performing teams in a matrix environment Role preferably based at the Princeton Pike site in Lawrenceville, NJ; travel ~20%-30% globally Note: If you come across a role that intrigues you but doesn’t perfectly line up with your resume, you’re encouraged to apply. You could be one step away from work that can transform your life and career.
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Senior Director, Immunology & Neuroscience (I&N), Medical Evidence Generation (MEG) role in Global Medical Affairs manages the evidence generation for the I&N portfolio (including Medical Affairs Sponsored studies [MAST], Clinical Research Collaborations [CRC], and investigator-sponsored studies [ISR]) and provides leadership for the cross-functional teams executing on the book of work. The I&N MEG Senior Director leads cross-functional matrix teams to build relationships and source research concepts addressing critical evidence gaps for assets in prioritized indications. The Senior Director reports to the Immunology & Neuroscience Executive Director. Responsibilities include: Build, manage, and coach a sustained high-performance, externally focused global team accountable for defining and executing the I&N portfolio to address key data gaps Coach a team of MEG Leads, including Clinical Scientists and Clinical Trial Physicians, in oversight of Medical clinical trials end-to-end (start-up, governance, contract negotiation and execution, oversight, and readout support) Design and drive strategies to identify and advance new medical trials that accelerate the development of the BMS pipeline Demonstrate experience in clinical concept development and partnering across the drug development continuum Lead cross-functional teams on scientific and study-related activities to ensure robust results Contribute to the evolution of the MEG organizational model and operational infrastructure Accountable for the I&N MEG book of work (MASTs, ISRs, CRCs, IEP development) ensuring alignment with the Integrated Evidence Plan (IEP) and timely, rigorous execution Oversee medical study protocol and ICF development with input to ensure clinical relevance, scientific rigor, patient safety, and alignment with study objectives Maintain scientific integrity and data quality during trial execution across all phases Co-develop and maintain IEPs with Medical, HEOR, Development and other stakeholders Partner with Medical Affairs and Drug Development to ensure cohesiveness and a single MEG voice Apply business acumen and fiscal stewardship to drive scientific value and allocate resources per company priorities Assist in concept reviews through the RFP process, providing context for ongoing work, areas of interest, and upcoming readouts Qualifications & Experience MD preferred (or international equivalent) 5+ years of clinical trial experience in the pharmaceutical industry (e.g., Clinical Trial Physician, Clinical Scientist); proficiency in drug development and managing company-sponsored trials and leading teams 5+ years of strategic leadership experience in pharma, with understanding of clinical and business development, Medical Affairs, and related functions 10+ years of experience in clinical science or clinical research Strong communication, leadership, and collaboration skills; ability to influence decisions at all levels Experience building and leading high-performing teams in a matrix environment Role preferably based at the Princeton Pike site in Lawrenceville, NJ; travel ~20%-30% globally Note: If you come across a role that intrigues you but doesn’t perfectly line up with your resume, you’re encouraged to apply. You could be one step away from work that can transform your life and career.
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