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) strategy Collect and synthesize internal and external insights to inform the USMA strategy and develop actions based on insight themes Provide 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 input Build 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 congresses Planning, organization and delivery of hematology HQ-led sessions at internal meetings Represent USMA as part of key internal meetings/workstreams including investigator sponsored trial reviews, medical strategy team and integrated brand team Lead external interactions with stakeholders including key external experts, advisory boards, academic groups, scientific societies, and patient advocacy groups Build and Maintain US External Expert network in collaboration with the asset leads Develop and execute Key External Experts (KEE) engagement plans Hematology Training Lead (Medical & Commercial as needed) Assist in publication strategy and support Integrate 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…