Director, Medical Development, Precision Oncology

Abbott

. Develop the overall vision and strategy for Exact Sciences’ Precision Oncology products, including Oncotype DX, OncoExTra, therapy selection, and molecular residual disease portfolios .

Posted 11/9/2026full-timeRemote • California • United StatesLead💰 $149,300 - $298,700 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Precision Oncology product development and commercialization, with a strong focus on molecular oncology and cross-functional team leadership. Proven ability to engage with oncology leaders and manage complex projects within the pharmaceutical and biotech industries.

Highest-signal resume keywords

M.D. Or D.O. In A Related FieldFellowship Training In OncologyExpertise In Molecular OncologyExperience In Oncology Within Pharmaceutical Or Biotech IndustryKnowledge Of FDA And Ex-U.S. Regulatory Processes

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Applicant Tracking System Keywords

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Hard Skills

Clinical Protocol DevelopmentMolecular Diagnostics DevelopmentLaboratory Analytical Process DevelopmentBiostatisticsProduct Commercialization StrategiesClinical Trial ManagementOncology Therapeutics DevelopmentData InterpretationScientific Presentation SkillsRegulatory Documentation

Soft Skills

LeadershipCollaborationCommunicationAnalytical ThinkingInclusion Mindset

Industry Keywords

Precision OncologyOncotype DXOncoExTraCheckpoint Inhibitor TherapiesClinical ResearchTranslational ResearchQuality Management SystemPharma PartnershipsAdvisory BoardsClinical Utility

About the role

Key responsibilities & impact

Develop the overall vision and strategy for Exact Sciences’ Precision Oncology products, including Oncotype DX, OncoExTra, therapy selection, and molecular residual disease portfolios
Identify opportunities to expand indications for existing Precision Oncology products and develop new products within the pharma space
Provide medical expertise for commercialization strategies and product profiles for new products and services
Serve as medical monitor on study teams and lead clinical protocols supporting product development, validation, and commercialization
Engage oncology leaders to understand clinical questions, identify clinical tool needs, and communicate the scientific validity and clinical utility of products
Lead scientific presentations and publications resulting from product development collaborations
Provide oncology expertise and clinical insight to cross-functional teams throughout the lifecycle of genomic tests and services
Build and lead internal and external collaborations with academic oncology leaders, cooperative trial groups, research organizations, investigators, and clinical trial sites
Initiate and lead external advisory boards involving pharma medical leaders, key opinion leaders, and other third parties
Review and interpret key study results and lead reporting
Design and implement medical support for new or extended precision oncology tests and services
Lead and participate in cross-functional teams spanning business development, research and development, pathology, clinical laboratory operations, biostatistics, clinical affairs, medical affairs, regulatory, market access, and commercial functions
Identify pharma partners for new product opportunities and indication expansion
Support continuous improvement of team leadership practices, communications, interviewing, team building, and Precision Oncology culture
Apply analytical, communication, prioritization, collaboration, and quality-focused practices
Support and comply with Quality Management System policies and procedures
Maintain regular and reliable attendance
Travel as required

Requirements

What you’ll need

M.D. or D.O. in a related field as outlined in the essential duties
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 act with an inclusion mindset and model these behaviors for 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 typical working day

Benefits

Comp & perks

Travel up to 30% of working time may include overnight/weekend travel
Equal Opportunity Employer protections for Minorities/Women/Individuals with Disabilities/Protected Veterans