• Lead and provide scientific leadership and support for compounds in various stages of clinical development, as well as approved products in the Hematology/Oncology and Solid Tumor Therapeutic Areas.
• This individual will be involved in integrated strategic planning and execution within Global Medical and Scientific Affairs (GMSA), as well as with partners in the US Commercial organization, Research and Development and Market Access, and will lead medical affairs activities for Hematologic Malignancies / Solid Tumors.
• He/she will represent GMSA in hematologic malignancies and solid tumor initiatives with broad responsibilities and impact across the US business and overall GMSA organization. Particularly, he/she will work closely with the Global Medical Affairs and cross-functional Program Teams to support and prepare for the US launch of new products and label expansion.
• Lead and support development and execution of medical strategies in close collaboration with Program Team members within the assigned therapeutic area(s).
• Ensure the development of effective evidence generation strategies, medical education, scientific communication strategies and training to drive launch excellence.
• Partner with GMSA leads, as well as cross-functional leaders in Research and Development and Commercial to lead and execute medical tactics in the assigned therapeutic area that is aligned with the Brand strategy.
• Supports the development of robust publication and congress strategies for assigned therapeutic areas in partnership with cross-functional leads.
• Serve as lead for major congresses, ensuring cross-functional alignment and execution in relevant therapeutic areas.
• Lead and support the development of a robust engagement strategy with Oncology thought leaders and build advocacy with top-tier individuals.
• Work closely with Field Based Medical Affairs on training, messaging, and prioritization of field activities to ensure successful execution of tactics supporting the overall medical strategy.
• Generate actionable insights to aid the medical, clinical and marketing teams to identify gaps and influence drug/brand development.
• Serve as the subject matter expert for internal and external programming, including symposia, advisory boards, and steering committees.

• Experience and understanding of oncology drug development.
• Previous pharmaceutical industry experience required.
• Prior medical affairs experience, minimum 5 years preferred.
• Advanced degree (MD, PharmD or PhD) in health-related field with experience in Hematology/Oncology and Solid Tumors, preferably gynecological cancers.
• Knowledgeable of competitive products and their application.
• Strong expertise in the conduct of clinical trials in hematology/oncology and solid tumors, with proficiency in critical data review and interpretation.
• Product lifecycle management experience highly preferred.
• Good understanding of Medical Affairs and comprehensive understanding of the compliance issues concerning MA function.
• Support successful cross-functional and multi-disciplinary teams in changing competitive environment, changing product technology, and changing customer needs.
• Excellent communication and organization skills, including presentations to large groups, facilitation of interactive discussions, and 1:1 scientific discussions with thought leaders.
• Demonstrated customer focus orientation & credibility with customers.
• Knowledge/application of data sources, reports and tools for the creation of solid plans.
• Ability to successfully collaborate in a diverse work group, motivate and maximize productivity.
• Excellent analytical, communication and presentation skills and solid experience in translating medical/clinical information into medical affairs strategies.
• Ability to think strategically, good leadership skills, efficiently manage time and priorities, and able to work in a fast-paced, ever-changing environment.
• Collaborative mindset, good communication skills
• Travel requirement; approximately 20% (including international)

Our Karyopharmers live and demonstrate our ICARE values every day!

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  A fun, collaborative, work environment
• A culture of employee engagement, diversity, and inclusion
• Competitive salary, bonus, and generous equity offerings (RSU’s-at time of offer and annual awards) – we are partners in prosperity!
• Peace of mind through best in class medical (deducible paid by KPTI), dental, vision, disability, and life insurance, parental leave, a matching 401k program (immediate vesting), and tuition reimbursement.
• Generous PTO and Holidays – we encourage you to recharge and spend time with family and friends.
• Ample opportunities to learn and take on new responsibilities in a fast-paced, and patient focused company. (tuition reimbursement, management development programs, and a variety of reward and recognition programs)
• Cell phone allowance

• Karyopharm requires all employees to be fully vaccinated against the Covid19 virus at the time of employment

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  This position is eligible for remote/hybrid working arrangement (may work from home/virtually; may also work hybrid on-site-virtual as required/approved by hiring manager.