Director, Medical Development, Precision Oncology

This is a fully remote position, open to applicants in California.

📋 Description

• Formulate the comprehensive vision and strategy for Exact Sciences’ Precision Oncology offerings, such as Oncotype DX, OncoExTra, therapy selection, and molecular residual disease portfolios.

• Discover opportunities to broaden indications for current Precision Oncology products and innovate new products within the pharmaceutical sector.

• Offer medical expertise to shape commercialization strategies and product profiles for new offerings and services.

• Act as a medical monitor on study teams and spearhead clinical protocols that support product development, validation, and commercialization.

• Collaborate with oncology leaders to comprehend clinical inquiries, pinpoint clinical tool requirements, and convey the scientific credibility and clinical value of products.

• Direct scientific presentations and publications that emerge from product development partnerships.

• Provide oncology knowledge and clinical perspectives to cross-functional teams throughout the lifespan of genomic tests and services.

• Establish and manage collaborations with both internal and external academic oncology leaders, cooperative trial groups, research organizations, investigators, and clinical trial sites.

• Initiate and oversee external advisory boards that include pharma medical leaders, key opinion leaders, and other stakeholders.

• Analyze and interpret significant study outcomes and guide reporting efforts.

• Create and execute medical support for new or enhanced precision oncology tests and services.

• Lead and engage in cross-functional teams that encompass business development, research and development, pathology, clinical laboratory operations, biostatistics, clinical affairs, medical affairs, regulatory, market access, and commercial functions.

• Identify pharmaceutical partners for new product opportunities and the expansion of indications.

• Promote ongoing enhancement of team leadership practices, communication skills, interviewing techniques, team building, and the culture of Precision Oncology.

• Employ analytical, communication, prioritization, collaboration, and quality-oriented practices.

• Ensure compliance with Quality Management System policies and procedures.

• Maintain consistent and dependable attendance.

• Travel as necessary.

⛳️ Requirements

• M.D. or D.O. in a relevant field as outlined in the essential duties.

• Completion of fellowship training or its equivalent in oncology.

• Proven expertise in molecular oncology.

• Demonstrated capability to lead cross-functional internal and external teams of professionals focused on complex, multifaceted projects.

• Familiarity with laboratory analytical process development and biostatistics.

• Proven ability to carry out the essential duties of the position with or without accommodation.

• Authorization to work in the United States without the need for sponsorship.

• Preferred: Over 2 years of experience in healthcare.

• Preferred: Background in oncology within the pharmaceutical or biotech industry, particularly in clinical or translational research.

• Preferred: Experience with checkpoint inhibitor therapies.

• Preferred: Involvement in the development of new oncology therapeutics and molecular diagnostics.

• Preferred: Strong understanding of FDA and Ex-U.S. regulatory documentation and processes.

• Ability to operate with an inclusive mindset and exemplify these behaviors within the organization.

• Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a standard working day.

🏝️ Benefits

• Travel up to 30% of working time may include overnight/weekend travel.

• Equal Opportunity Employer protections for Minorities/Women/Individuals with Disabilities/Protected Veterans.