
Scientific Director, Medical Affairs
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in United States.
β’ Act as a therapeutic area expert in TIL cell therapy for educational, strategic, and tactical discussions and presentations.
β’ Assist and educate healthcare providers to enhance tumor tissue starting material for the manufacturing of lifileucel.
β’ Facilitate engagement and discussions on best practices with surgeons regarding tumor tissue procurement.
β’ Support the ATC medical onboarding process for direct patient care and provide continuous assistance for patient- and product-specific inquiries.
β’ Function as a subject matter expert and clinical support for TIL cell therapy.
β’ Offer clinical trial assistance by collaborating with surgeons involved in Iovance and investigator-sponsored trials.
β’ Represent Medical Affairs in both internal and external settings, including US and global cross-functional teams, consultants, advisory boards, and steering committees.
β’ Work in collaboration with Commercial Quality, Market Access, Clinical Development, and Medical Affairs teams.
β’ Engage in Medical Affairs cross-functional working groups.
β’ Represent Iovance at professional meetings, congresses, and local symposia.
β’ Review disease strategy plans, presentations, manuscripts, educational materials, IIT protocols, committee and advisory board objectives, response letters, and commercial brand strategies.
β’ Collaborate with Scientific Communications on publication strategies, gap analyses, and key messaging.
β’ Interact with internal stakeholders such as Medical Affairs, ATC Operations, Commercial, Clinical Science and Operations, Research Alliances, Manufacturing, Quality, Marketing, Market Access, Regulatory Affairs, Project Management, and Training.
β’ Engage with external investigators, KOLs, non-physician HCPs, steering committees, and advisory boards.
β’ A Physician Assistant or Nurse Practitioner with clinical or surgical experience is essential; experience in melanoma, cellular therapy, and/or surgical oncology is highly preferred.
β’ A degree from an accredited and recognized institution is mandatory.
β’ At least 7-10 years of experience in academia or industry is strongly preferred.
β’ Proficiency in conducting clinical trials in hematology/oncology is highly desirable.
β’ Outstanding oral and written communication abilities, including delivering presentations to large audiences, facilitating interactive discussions, and engaging in one-on-one interactions with surgeons and other healthcare professionals.
β’ Strong analytical skills with a history of translating medical, clinical, and surgical information into Medical Affairs strategies.
β’ Expertise in critical data review and interpretation, especially in evaluating surgical variables that affect product quality and outcomes.
β’ A proven customer-focused approach and credibility with clients.
β’ Strong strategic thinking and analytical capabilities.
β’ Experience in developing scientific content and proficiency in using PowerPoint for presentations.
β’ Knowledge and application of data sources, reports, and tools for creating plans related to surgical workflows and tumor procurement metrics.
β’ Willingness and ability to travel as required, primarily within the United States.
β’ Capacity to remain stationary, whether standing or sitting, for extended periods.
β’ Ability to navigate within an office environment and exert up to 10 pounds of force occasionally or negligible force frequently or constantly.
β’ Visual acuity for preparing and analyzing data and figures, viewing computer screens, and extensive reading.
β’ Capability to perform repetitive motions with wrists, hands, and fingers.
β’ Ability to communicate effectively with others to exchange information.
β’ Clear and conceptual thinking skills, excellent judgment, troubleshooting abilities, problem-solving acumen, discretion, stress management, multitasking, and deadline management capabilities.
β’ Remote office environment
β’ Equal-opportunity and inclusive work environment
β’ Reasonable accommodations available upon request
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