Oncologist, Medical Director, Clinical Development

Labcorp

Medical Director advancing Labcorp Oncology’s solid-tumor MRD and ctDNA diagnostics. Leading clinical evidence, product strategy, reimbursement support, and precision-oncology adoption.

Posted 8/13/2026full-timeDurham • North Carolina • 🇺🇸 United StatesLead💰 $250,000 - $360,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical development strategy, particularly in MRD and ctDNA technologies, with a strong focus on clinical trial design, evidence generation, and regulatory compliance. Proven ability to lead cross-functional teams and build strategic relationships within the oncology landscape.

Highest-signal resume keywords

M.D. Or D.O. DegreeBoard Certification In Medical OncologyClinical Trial DesignOncology Clinical DevelopmentEvidence-Generation Methodologies

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study DesignProtocol DevelopmentEndpoint SelectionData AnalysisBiostatisticsRegulatory RequirementsEpidemiologyPublication PlanningSolid-Tumor Treatment ParadigmsClinical Guidelines

Soft Skills

Strategic ThinkingProject LeadershipOrganizational SkillsExcellent Written CommunicationPresentation Skills

Certifications & Qualifications

Board Certification In Medical Oncology

Industry Keywords

MRD PortfolioCtDNA TechnologiesClinical DevelopmentOncologyBiotechnologyDiagnosticsCROAcademic ResearchHealth-System AdoptionClinical Care Pathways

About the role

Key responsibilities & impact

Lead clinical development strategy for Labcorp Oncology’s MRD portfolio across solid tumors
Develop and execute evidence-generation programs for MRD and ctDNA technologies
Lead clinical study design, protocol development, endpoint selection, study oversight, and interpretation of results
Direct clinical strategies for MRD detection, recurrence monitoring, treatment response, risk stratification, treatment selection, and clinical trial enrichment
Guide integration of MRD testing into clinical care pathways and routine oncology practice
Build relationships with principal investigators, cooperative groups, academic research centers, professional societies, payers, and other stakeholders
Provide medical leadership across the MRD product lifecycle from concept development through commercialization and lifecycle management
Advise on product development, assay development, biomarker strategy, clinical claims, validation requirements, and product roadmaps
Support payer coverage, reimbursement, guideline inclusion, and health-system adoption strategies
Represent Labcorp Oncology at scientific congresses, advisory boards, investigator meetings, and industry forums
Provide post-launch medical support, clinical education, scientific communications, and publication planning
Lead, mentor, and develop medical directors and disease-specific clinical leaders
Establish portfolio priorities, allocate resources, and align development objectives with organizational strategy
Collaborate with medical affairs, operations, biostatistics, regulatory, market access, legal, compliance, commercial, and R&D teams
Support regulatory submissions and monitor scientific, clinical, and competitive developments

Requirements

What you’ll need

M.D. or D.O. degree from an accredited medical school
Board certification in Medical Oncology
5 or more years of post-fellowship clinical experience treating patients with solid tumors
3 or more years of oncology clinical development, clinical research, clinical trial leadership, or evidence-generation experience in pharmaceutical, biotechnology, diagnostics, CRO, or academic research environments
8 or more years of experience designing, leading, or supporting prospective and/or retrospective clinical studies
Experience with protocol development, endpoint selection, study conduct, data analysis, interpretation, and publication of results
5 or more years of experience working cross-functionally with operations, biostatistics, regulatory affairs, medical affairs, R&D, commercial, and/or market access teams
20 or more presentations delivered to scientific congresses, investigators, KOLs, healthcare providers, advisory boards, or medical education forums
Strong understanding of oncology clinical trial methodology, study design, evidence generation, biostatistics, and regulatory requirements
Broad knowledge of solid-tumor treatment paradigms, clinical guidelines, biomarkers, and precision oncology
Ability to travel up to 30%
Expertise in clinical trial design, protocol development, biostatistics, epidemiology, and evidence-generation methodologies
Strong understanding of regulatory, compliance, and quality frameworks supporting clinical development and diagnostics
Ability to evaluate complex scientific and clinical data and translate insights into development strategy
Strong strategic thinking, portfolio management, project leadership, and organizational skills
Excellent written, verbal, and presentation skills
Ability to lead in highly matrixed organizations and influence without direct authority
Ability to manage multiple high-priority initiatives, navigate ambiguity, solve complex problems, and drive cross-functional alignment
Established relationships with oncology investigators, cooperative groups, academic cancer centers, and professional societies

Benefits

Comp & perks

Annual bonus under the Labcorp Bonus Plan
Discretionary short- and long-term incentive packages may be included
Medical insurance
Dental insurance
Vision insurance
Life insurance
Short-term disability (STD)
Long-term disability (LTD)
401(k)
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement
Employee Stock Purchase Plan