Bei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Veränderung des Lebens von Patienten durch Wissenschaft. In den Bereichen Onkologie, Hämatologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielfältigsten und vielversprechendsten Pipelines der Branche - trägt jeder unserer leidenschaftlichen Kollegen zu Innovationen bei, die bedeutende Veränderungen vorantreiben. Wir verleihen jeder Therapie, für die wir Pionierarbeit leisten, eine menschliche Note. Kommen Sie zu Bristol Myers Squibb und machen Sie einen Unterschied. Responsibilities will include, but are not limited to: • Strategic and Tactical Planning for Global Medical Affairs Cell Therapy success. • Launch plans for new cell products or new indication launches in the global Cell Therapy franchise in collaboration with relevant disease teams. • Cell Therapy integrated evidence generation plan implementation in specified region. • Cell Therapy publication plan development in partnership with Scientific Communications and relevant disease teams, including gap analysis, and key messages. • Oversee execution of Medical Affairs Cell Therapy Sponsored Trials in specified region, ensuring excellent standards on compliance, quality, timeliness, budget, and Medical governance. • Represent Global Medical Affairs as Cell Therapy expert in both internal and external venues including regional and Global cross-functional teams, clinical sub-teams, advisory boards, steering committees, investigator meetings, congresses, and local symposia. • Collaborate with country Medical Affairs colleagues to define, guide and execute Cell Therapy regional strategies and tactics with appropriate use of resources. • Provide high quality medical input and review of: Cell Therapy strategy plans, abstracts, posters, slides, manuscripts, educational materials, IIT protocols, steering committee and advisory board meeting objectives, Medical information letters, Commercial Brand plans, Scientific educational grant requests and patient advocacy grant requests in collaboration with cross-functional teams. • Track priority Cell Therapy medical plans in specified EU region and performance against goals/budget. • Perform research and analytics and provide recommendations to support quality medical decisions regarding Cell Therapy clinical research, consultancy, and internal planning. • Participate in Cell Therapy data summaries, preparation for site visits/corporate visits presentations in collaborations with Major Markets. Interact with key stakeholders, as a Cell Therapy medical strategy expert. Internal, including and not limited to: • Medical Affairs partners in different therapeutic areas • Global Medical Affairs Leadership • Major Markets • Market Access • Clinical R&D • Statistics • Translational Research • Regulatory Affairs • Project Leadership External, including and not limited to: • Investigators, KOLs • Global steering committees • Scientific Advisory Boards • Advocacy groups • Cooperative groups The ideal candidate will have: • Medical Degree, preferably board certified in Hematology/Oncology • Expertise in hematopoietic cell therapy and/or transplantation is a strong plus • A minimum of 3-5+ years industry experience • Expertise in the conduct of clinical trials in hematology/oncology • Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies • Proficiency in critical data review and interpretation • Excellent oral and written communication skills, including presentations to large groups, facilitation of interactive discussions, and 1:1 discussion with thought leaders • Knowledge/application of data sources, reports, and tools for the creation of solid plans Expected Areas of Competence: • Medical lead of clinical studies, with demonstrated decision making capabilities • Medical and scientific expertise in Cell Therapy sharing with cross-functional colleagues • Ability to present clearly in scientific and clinical settings • Conduct of medical data review of trial data, including eligibility review. • Site onboarding support in partnership with country medical and cross functional teams for Cell Therapy questions and education (including safety management guidelines) • Assessment of key safety-related serious adverse events in partnership with GPVE. • Provide medical strategic input in protocol development (input on inclusion/exclusion criteria and other safety-related clinical considerations). • Fulfill GCP and compliance obligations for clinical conduct and maintain all required training for same. • Support executional delivery of studies (eg, site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc). • Identify and build relationships with principal investigators. Identify and cultivate thought leaders (TLs) to gain their inputs on emerging science in Cell Therapy biomarker research, disease knowledge and design of Cell Therapy clinical development studies and programs. • Maintain a strong medical/scientific reputation within Cell Therapies. • Keep informed of development and regulatory issues related to other competitive or relevant compounds in development that may impact Cell Therapy portfolio within the competitive landscape. • Provide ongoing Cell Therapy medical education, protocol specific training, to support Cell Therapy study team, investigators, and others. Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, as inclusion and integrity bring out the highest potential of each of our colleagues. 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. Wir setzen uns auf der ganzen Welt leidenschaftlich dafür ein, das Leben von Patienten mit schweren Krankheiten zu beeinflussen. Unsere gemeinsamen Werte Leidenschaft, Innovation, Dringlichkeit, Verantwortlichkeit, Inklusion und Integrität befähigen uns, unsere individuellen Talente und unterschiedlichen Perspektiven in einer integrativen Kultur einzusetzen und bringen das höchste Potenzial jedes unserer Kollegen hervor. Bristol Myers Squibb weiß um die Bedeutung von Balance und Flexibilität im Arbeitsumfeld. Wir bieten daher eine Vielzahl von attraktiven Benefits, Dienstleistungen und Programmen an, die unseren Mitarbeitern die Ressourcen bieten, ihre Ziele sowohl bei der Arbeit als auch in ihrem Privatleben zu verfolgen.