Medical Director – Clinical Development, MRD Portfolio, Solid Tumors

🔥 0 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $320k - $340k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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Labcorp

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1969

💼 Consulting

📦 Logistics

🏥 Healthcare

💰 Post-IPO Debt on 2019-06

Consulting • Logistics • Healthcare

Labcorp is a leading global life sciences company that provides comprehensive clinical laboratory and end-to-end drug development services. The company offers a wide range of diagnostic tests and services for patients, providers, and biopharmaceutical companies. Labcorp specializes in areas such as oncology, women's health, neurology, and genetics, offering both routine and specialized laboratory testing. It supports healthcare systems and organizations with clinical lab testing, health assessments, and employee wellness programs. Labcorp also plays a significant role in the biopharma sector, providing nonclinical research, central laboratory services, and consulting for drug development and commercialization. With their commitment to science and innovation, Labcorp aims to improve health and change lives worldwide.

📋 Description

• Serve as the clinical development lead for Labcorp Oncology's MRD portfolio across solid tumors • Develop and execute clinical development strategies for MRD and ctDNA-based technologies • Lead medical design and clinical oversight of evidence-generation programs • Drive alignment across internal stakeholders involved in clinical studies, evidence generation, and product development • Translate emerging clinical data into recommendations for portfolio strategy, indication expansion, product development, and clinical adoption • Serve as senior clinical subject matter expert for MRD technologies and applications • Support investigator-initiated studies, strategic research collaborations, and real-world evidence programs • Provide medical leadership for the MRD portfolio from concept development through commercialization and lifecycle management • Define clinical evidence requirements, intended-use populations, clinical claims, validation strategies, and evidence-generation priorities • Guide assay development, biomarker strategies, and next-generation technology initiatives • Evaluate competitive technologies, emerging biomarkers, and standards of care • Develop evidence-generation strategies supporting payer coverage, reimbursement, and health-system adoption • Provide leadership for studies demonstrating clinical utility, physician decision-making impact, patient outcomes, and economic value • Support interactions with payers, policy stakeholders, and guideline organizations • Build relationships with oncology investigators, academic medical centers, cooperative groups, professional societies, and industry partners • Represent Labcorp Oncology at congresses, advisory boards, investigator meetings, and external scientific forums • Provide post-launch medical support and clinical guidance regarding MRD testing • Develop educational content, manuscripts, abstracts, presentations, congress submissions, and publications • Align stakeholders around clinical development priorities, evidence-generation plans, and portfolio objectives • Mentor colleagues and provide scientific guidance to project teams and stakeholders • Collaborate across Medical Affairs, Clinical Development, Operations, Biostatistics, Regulatory Affairs, Market Access, Commercial, Legal, Compliance, and R&D • Support regulatory submissions and interactions through clinical expertise and scientific rationale • Monitor emerging scientific, clinical, technological, and competitive developments

🎯 Requirements

• 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 within the pharmaceutical, biotechnology, diagnostics, CRO, or academic research environment • 8 or more years of experience designing, leading, or supporting prospective and/or retrospective clinical studies, including protocol development, endpoint selection, study conduct, data analysis, interpretation, and publication of results • 5 or more years of experience working in cross-functional environments with operations, biostatistics, regulatory affairs, medical affairs, research & development, commercial, and/or market access teams • 20 or more presentations delivered to scientific congresses, investigators, key opinion leaders (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 approaches • Ability to travel up to 30% • Expertise in clinical trial design, protocol development, biostatistics, epidemiology, and evidence-generation methodologies • Preferred: 5 or more years of experience in molecular diagnostics, liquid biopsy, MRD, ctDNA, precision oncology, or biomarker-driven clinical development • Preferred: 5 or more years of industry experience within diagnostics, biotechnology, pharmaceutical, or life sciences organizations • Preferred: 3 or more years serving as a medical lead, clinical development lead, or equivalent leadership role • Preferred: 5 or more years leading oncology clinical development programs across multiple solid tumor indications • Preferred: 3 or more studies supporting clinical utility, reimbursement, payer coverage, guideline inclusion, or adoption • Preferred: 3 or more years partnering with Market Access teams • Preferred: 3 or more years of direct people leadership experience • Preferred: 20 or more peer-reviewed publications, scientific presentations, and participation at major oncology congresses • Preferred: Participation in 2 or more regulatory submissions, product launches, or lifecycle management initiatives

🏖️ Benefits

• Annual bonus under the Labcorp Bonus Plan • Discretionary short- and long-term incentive packages • 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