Director, Worldwide Medical Oncology, Medical Communications

Overview Director, Worldwide Medical Oncology, Medical Communications Position reports to the Director of Thoracic, H&N Medical Communications within WWMO, Global Medical Affairs and is responsible for the strategy and execution of medical communication plans for Pumitamig (BNT327/BMS986545) across multiple potential therapy areas (e.g., lung, breast, GI). Responsibilities Alliance Partnership: Collaborate with the alliance partner to drive joint initiatives, ensure alignment on strategic objectives, and facilitate communication across cross-functional teams. Medical Communications Strategy: Establish a clear, viable, and compelling strategy for TA-specific Medical Communications; ensure delivery of timely medical publications, scientific content, medical education and congress presentations worldwide; chair the Medical Communications Working Group and deliver the 3-year strategic/18-month tactical Medical Communications plan and related outputs. Scientific Narrative & Platform: Develop, pull-through and execute the Scientific Narrative aligned with portfolio strategy; manage publication plans, content plans, and the Scientific Communication Platform. Content Development & Submissions: Lead development of personalized medical communications and ensure timely journal submissions, publications, Congress presentations, and delivery of internal and external scientific content. Digital & AI-Driven Innovation: Leverage digital, omnichannel tools, and AI-driven solutions to enhance Medical Communications strategies and engagement with healthcare professionals and stakeholders. Budget & Resource Management: Manage assets/indication-level budgets and allocate resources to highest business priorities; interface with matrix partners for trade-offs. Data Dissemination & Science Leadership: Serve as subject matter expert on asset/indication communication landscapes, data disclosure/dissemination, and representation to external investigators and editors; drive adherence to Good Publication Practices and industry standards. Process Improvement & Standards: Lead internal process improvements to ensure ethical and credible publication practices; align plans with major markets and trial milestones; ensure data integrity and transparency. Stakeholder Engagement: Build collaborative relationships with academic and clinical experts, publishers, medical associations, customers, and internal stakeholders; set metrics and communicate outcomes routinely. Qualifications & Experience Advanced scientific degree (PharmD, PhD or MD preferred). 8-10 years in Pharmaceutical/Healthcare with focus on medical communications; therapy area experience preferred. Proven strategic leadership, cross-functional collaboration, and ability to operate in ambiguous environments. Experience leading cross-cultural teams across matrix organizations and global geographies; strong program management and time-management skills. Track record of achieving business results in a complex corporate environment with tight timelines; ability to influence stakeholders and manage change. Experience across all phases of drug development and commercialization; ability to interpret trial data and translate into communications strategy. Strong negotiation, stakeholder engagement and communication skills; willingness to travel domestically and internationally. Preferred: CMPP or ISMPP active member; knowledge of GPP, ICMJE, Sunshine Act; publication management tools familiarity (e.g., iEnvision/DataVision). We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected veteran status. Reasonable accommodations may be available on request. #J-18808-Ljbffr