Scientific Director, Hematology

Overview:As a Scientific Director working on the US Medical Affairs team, you will be accountable for the external engagement strategy, medical education (CME, symposia, advisory boards), medical affairs resource development and training for tagraxofusp and the hematology pipeline. It is essential to establish strong partnerships with Commercial and Clinical stakeholders in establishing the strategy which is wholly aligned with the cross-functional plan. Excellent collaboration and exchange with countries and the Regions is crucial in order to ensure the execution of the global strategy at local level and to ensure that countries needs are reflected in the global strategy. Please note--this position is classified as a corporate office position. In accordance with the New York employer convenience rule, Stemline will withhold New York state income taxes for all corporate office employees, regardless of whether these employees work in New York or remotely. Responsibilities: Contribute to annual medical brand planning and the US Medical Affairs (USMA) strategyCollect and synthesize internal and external insights to inform the USMA strategy and develop actions based on insight themesProvide support and life cycle management for tagraxofusp and pipeline hematology assets Drive alignment on medical need within the organization to ensure maximal functional and regional/country inputBuild US medical tactics including US medical field resources and training Lead medical affairs hematology content development, adaptation and integrity (i.e. field materials)Drive medical affairs activity including at US hematology-oncology congressesPlanning, organization and delivery of hematology HQ-led sessions at internal meetingsRepresent USMA as part of key internal meetings/workstreams including investigator sponsored trial reviews, medical strategy team and integrated brand teamLead external interactions with stakeholders including key external experts, advisory boards, academic groups, scientific societies, and patient advocacy groupsBuild and Maintain US External Expert network in collaboration with the asset leadsDevelop and execute Key External Experts (KEE) engagement plansHematology Training Lead (Medical & Commercial as needed)Assist in publication strategy and supportIntegrate into workstreams with patient advocacy and CDx teams Qualifications: Advanced medical and/or scientific degree (e.g., MD/DO, PhD, PharmD, PA, NP)Minimum of 5 years combined oncology clinical, research and/or pharmaceutical/biotech industry experience, with medical affairs experience strongly preferred.Hematology experience required, knowledge of BPDCN and AML preferred.Experience with Medical Affairs platforms, systems and processes (e.g. Veeva CRM, PRC submission)Strategic Thinking: Ability to translate high-level business goals into practical, executable operational plans. Strong grasp of scientific accuracy and the ability to adapt complex field resources.Leadership & Influence: Exceptional ability to lead complex projects, influence stakeholders at all levels, and drive organizational change without direct reporting authority.Analytical Rigor: Proficient in data analysis, reporting, and utilizing metrics to drive improvements.Communication: Excellent verbal, written, and presentation skills.Detail-Oriented: Meticulous attention to detail with an unwavering focus on quality and compliance.Incumbent must have track record of working well in a dynamic environment and enjoy working with different stakeholders (clinical, pre-clinical, external customers, etc.)Knowledge and understanding of clinical priorities for different healthcare professionals including physicians, nurses, pharmacist, researchers and research associatesHistory of being successful in fast-paced, dynamic environment, self-motivated, works with limited supervisionAbility to execute both tactical and strategic work are requirements.Capability to work independentl