Bristol Myers Squibb
Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation
Bristol Myers Squibb, Madison, New Jersey, us, 07940
Overview
Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation at Bristol Myers Squibb. Oversees evidence generation for the Immunology & Neuroscience portfolio, including Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator-Sponsored Research Studies (ISRs). Aligns activities with internal strategies to accelerate pipeline development; fosters relationships with thought leaders and external partners; manages the lifecycle of CRCs and ISRs; collaborates with academic and professional networks to address evidence gaps. Responsibilities
Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, representing BMS as a trusted, inclusive, and innovative industry partner. Provide end-to-end oversight of Medical clinical trials (start-up, governance, agreements, execution, oversight, and readout). Contribute to clinical concept development and partnering across the drug development continuum. Deliver CRCs, ISRs, and MASTs from concept ideation through governance approval and throughout the study lifecycle. Serve as point of contact for CRCs, ISRs, and MASTs within Therapeutic and Disease Area teams. Design and drive strategies to accelerate development by leveraging external research platforms, technologies, and insights. Advise senior functional and therapeutic area leaders on external opportunities informing strategy and integrated evidence generation plans. Lead a limited number of high-visibility projects requiring disease area expertise. Contribute to the evolution of MEG therapeutic area strategy and value proposition. Position based at Lawrenceville (PPK) or Madison (GIR), New Jersey. Qualifications & Experience
Advanced scientific degree (MD, PhD, PharmD, MS or equivalent) with extensive relevant scientific/clinical experience. At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant commercial roles; prior customer-facing experience desirable. Proven ability to analyze data generation opportunities with minimal supervision and to build external thought-leader relationships. Strong communication and interpersonal skills to influence decisions at all levels; ability to balance business and scientific considerations with leadership. Understanding of global healthcare systems and academic settings; ability to lead in ambiguous and changing environments. Demonstrated project planning and management of clinical trials; ability to partner across functions and levels. Willingness to travel 20%-30% globally. Location
Based in New Jersey: Lawrenceville (PPK) or Madison (GIR).
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Director, MEG Lead Immunology & Neuroscience, Medical Evidence Generation at Bristol Myers Squibb. Oversees evidence generation for the Immunology & Neuroscience portfolio, including Clinical Research Collaborations (CRCs), Medical Affairs Sponsored Studies (MAST), and Investigator-Sponsored Research Studies (ISRs). Aligns activities with internal strategies to accelerate pipeline development; fosters relationships with thought leaders and external partners; manages the lifecycle of CRCs and ISRs; collaborates with academic and professional networks to address evidence gaps. Responsibilities
Facilitate collaborative exchange between BMS and thought leaders in community practice and academia, representing BMS as a trusted, inclusive, and innovative industry partner. Provide end-to-end oversight of Medical clinical trials (start-up, governance, agreements, execution, oversight, and readout). Contribute to clinical concept development and partnering across the drug development continuum. Deliver CRCs, ISRs, and MASTs from concept ideation through governance approval and throughout the study lifecycle. Serve as point of contact for CRCs, ISRs, and MASTs within Therapeutic and Disease Area teams. Design and drive strategies to accelerate development by leveraging external research platforms, technologies, and insights. Advise senior functional and therapeutic area leaders on external opportunities informing strategy and integrated evidence generation plans. Lead a limited number of high-visibility projects requiring disease area expertise. Contribute to the evolution of MEG therapeutic area strategy and value proposition. Position based at Lawrenceville (PPK) or Madison (GIR), New Jersey. Qualifications & Experience
Advanced scientific degree (MD, PhD, PharmD, MS or equivalent) with extensive relevant scientific/clinical experience. At least 5 years of experience in pharmaceutical clinical development, Medical Affairs, or relevant commercial roles; prior customer-facing experience desirable. Proven ability to analyze data generation opportunities with minimal supervision and to build external thought-leader relationships. Strong communication and interpersonal skills to influence decisions at all levels; ability to balance business and scientific considerations with leadership. Understanding of global healthcare systems and academic settings; ability to lead in ambiguous and changing environments. Demonstrated project planning and management of clinical trials; ability to partner across functions and levels. Willingness to travel 20%-30% globally. Location
Based in New Jersey: Lawrenceville (PPK) or Madison (GIR).
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