Bristol-Myers Squibb
Director, US Medical Affairs, Multiple Myeloma
Bristol-Myers Squibb, Madison, Wisconsin, us, 53774
Director, US Medical Affairs, Multiple Myeloma
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.The Medical Director, US Medical, Multiple Myeloma will report to the Senior Director, US Medical Multiple Myeloma Lead. He/she will provide medical leadership for a novel CELMoD asset and support for the overall Multiple Myeloma portfolio of products. This individual will be involved in integrated strategic planning within US Medical under the direction of the US Medical MM lead and MM/lymphoma disease lead as well as in close partnership with the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory, Translational Development, and Market Access, and will lead the US Medical asset strategy supporting the MM lead and the MM/Lymphoma Disease Lead.Key ResponsibilitiesStrategic and Tactical Planning: Responsible for the US Medical Affairs plans, in coordination with the Global Medical Affairs and other cross-functional teams.Represent US Medical Affairs as a therapeutic area expert in both internal and external venues including the US and Global cross-functional teams, clinical sub-teams, and advisory boards / steering committees. Represent BMS at professional meetings, congresses, and local symposia.Lead pre-launch and launch activities for key late-stage asset(s) entering the market.Lead/support various Medical Affairs cross-functional working groups. Collaborate with Medical Affairs field colleagues to define, guide and execute therapeutic regional strategies and tactics with appropriate use of resources.Responsible for the planning and timely execution of Medical Affairs Sponsored Trials, within appropriate standards for compliance, quality, timeliness, and budget.Responsible for the evaluation and support of investigator-initiated trials.Provide high-quality clinical input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, Investigator Sponsored Research (ISR) protocols, steering committee and advisory board meeting materials, Medical Information response documents, Scientific educational grant requests, and patient advocacy grant requests, etc.Track priority Medical Affairs tactics and performance to goals/budget.QualificationsExperience in Multiple Myeloma required. Advanced degree in health-related field such as MD, PharmD, or PhD, et al.A minimum of 5 years industry experience strongly preferred.Experience in the conduct of clinical trials in hematology/oncology.Proficiency in clinical data review and interpretation.Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies.Excellent oral and written communication skills. Matrix leadership of cross-functional teams.Demonstrated customer focus orientation & credibility with customers.Knowledge/application of data sources, reports, and tools for the creation of solid plans.Regular travel required as needed.
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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.The Medical Director, US Medical, Multiple Myeloma will report to the Senior Director, US Medical Multiple Myeloma Lead. He/she will provide medical leadership for a novel CELMoD asset and support for the overall Multiple Myeloma portfolio of products. This individual will be involved in integrated strategic planning within US Medical under the direction of the US Medical MM lead and MM/lymphoma disease lead as well as in close partnership with the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory, Translational Development, and Market Access, and will lead the US Medical asset strategy supporting the MM lead and the MM/Lymphoma Disease Lead.Key ResponsibilitiesStrategic and Tactical Planning: Responsible for the US Medical Affairs plans, in coordination with the Global Medical Affairs and other cross-functional teams.Represent US Medical Affairs as a therapeutic area expert in both internal and external venues including the US and Global cross-functional teams, clinical sub-teams, and advisory boards / steering committees. Represent BMS at professional meetings, congresses, and local symposia.Lead pre-launch and launch activities for key late-stage asset(s) entering the market.Lead/support various Medical Affairs cross-functional working groups. Collaborate with Medical Affairs field colleagues to define, guide and execute therapeutic regional strategies and tactics with appropriate use of resources.Responsible for the planning and timely execution of Medical Affairs Sponsored Trials, within appropriate standards for compliance, quality, timeliness, and budget.Responsible for the evaluation and support of investigator-initiated trials.Provide high-quality clinical input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, Investigator Sponsored Research (ISR) protocols, steering committee and advisory board meeting materials, Medical Information response documents, Scientific educational grant requests, and patient advocacy grant requests, etc.Track priority Medical Affairs tactics and performance to goals/budget.QualificationsExperience in Multiple Myeloma required. Advanced degree in health-related field such as MD, PharmD, or PhD, et al.A minimum of 5 years industry experience strongly preferred.Experience in the conduct of clinical trials in hematology/oncology.Proficiency in clinical data review and interpretation.Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies.Excellent oral and written communication skills. Matrix leadership of cross-functional teams.Demonstrated customer focus orientation & credibility with customers.Knowledge/application of data sources, reports, and tools for the creation of solid plans.Regular travel required as needed.
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