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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in molecular oncology and the ability to lead cross-functional teams in the development and commercialization of precision oncology products. Strong knowledge of FDA regulatory processes and experience in clinical or translational research within the pharmaceutical or biotech industry are essential.
Highest-signal resume keywords
M.D. Or D.O. In A Related FieldExpertise In Molecular OncologyExperience In Oncology Within Pharmaceutical Or Biotech IndustryKnowledge Of FDA Regulatory DocumentationLeadership In Cross-Functional Teams
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Protocol DevelopmentMolecular Diagnostics DevelopmentLaboratory Analytical Process DevelopmentBiostatisticsOncology Therapeutics DevelopmentCheckpoint Inhibitor TherapiesCommercialization StrategyProduct Profile DevelopmentScientific PresentationsClinical Trial Management
Soft Skills
Analytical SkillsCommunication SkillsCollaboration SkillsPrioritization SkillsResults-Driven Mindset
Industry Keywords
Precision OncologyClinical ResearchTranslational ResearchRegulatory ComplianceOncology Medical LeadersExternal Advisory BoardsPharmaceutical PartnershipsClinical UtilityGenomic TestsQuality Management System
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- Travel opportunity, including overnight/weekend travel
- Equal Opportunity Employer