Director, Medical Development, Precision Oncology

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🔥 1 hour ago

🏄 California – Remote

🏄 California – Remote

💵 $149.3k - $298.7k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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📋 Description

• Develop the overall vision and strategy for Exact Sciences’ Precision Oncology products and portfolios • Identify opportunities to expand indications for existing products and develop new products within the pharma space • Collaborate with research and development, pipeline, commercial, compliance, and regulatory stakeholders on commercialization strategy and product profiles • Serve as medical monitor on study teams and lead clinical protocol development supporting product development, validation, and commercialization • Engage oncology medical leaders to understand clinical questions, identify clinical tool needs, and communicate scientific validity and clinical utility • Lead scientific presentations and publications resulting from product development collaborations • Provide oncology expertise and clinical insight across the lifecycle of genomic tests and services • Lead and participate in cross-functional internal program teams and working groups across business development, R&D, pathology, clinical laboratory operations, biostatistics, clinical affairs, medical affairs, regulatory, market access, and commercial functions • Develop external relationships with academic oncology leaders, cooperative trial groups, research organizations, investigators, and clinical trial sites • Initiate and lead external advisory boards involving pharmaceutical medical leaders, key opinion leaders, and other third parties • Review, interpret, and lead reporting of key study results • Help design and implement medical support for new or extended precision oncology tests and services • Identify pharma partners for new product opportunities and indication expansion • Drive continuous improvement of team leadership practices and Precision Oncology culture • Apply analytical, communication, collaboration, prioritization, and results-driven skills • Support and comply with company Quality Management System policies and procedures • Maintain regular and reliable attendance and uphold company mission and values

🎯 Requirements

• M.D. or D.O. in a related field • Completion of fellowship training or equivalent in oncology • Demonstrated expertise in molecular oncology • Demonstrated ability to lead cross-functional internal and external teams of professionals focused on complex, multi-faceted projects • Familiarity with laboratory analytical process development and biostatistics • Demonstrated ability to perform the essential duties of the position with or without accommodation • Authorization to work in the United States without sponsorship • Preferred: 2+ years of experience in healthcare • Preferred: Experience in oncology within the pharmaceutical or biotech industry with an emphasis on clinical or translational research • Preferred: Experience working with checkpoint inhibitor therapies • Preferred: Experience in the development of new oncology therapeutics and molecular diagnostics • Preferred: Strong knowledge of FDA and Ex-U.S. regulatory documentation and processes • Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day • Ability to travel up to 30% of working time away from work location, may include overnight/weekend travel

🏖️ Benefits

• Travel opportunity, including overnight/weekend travel • Equal Opportunity Employer

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