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Clinical Program Director – Precision Oncology Diagnostics, MRD Focus
LabcorpClinical Program Director responsible for precision oncology diagnostics development at Labcorp. Leading clinical evidence generation and collaboration across medical, regulatory, and commercial teams.
Posted 7/17/2026full-timeRemote • North Carolina • 🇺🇸 United StatesLead💰 $160,000 - $180,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in designing and executing clinical development programs for precision oncology diagnostics, with a strong focus on regulatory strategy and compliance. Proven ability to lead scientific communication and establish partnerships for high-quality study execution.
Highest-signal resume keywords
Clinical DevelopmentPrecision Oncology DiagnosticsRegulatory StrategyReal-World Evidence GenerationGenetic Counseling
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 Utility StudiesStudy ExecutionOncology StudiesGuideline DevelopmentEvidence Dissemination
Soft Skills
LeadershipCollaborationCommunication
Certifications & Qualifications
Master’s Degree in Certified Genetic Counseling
Industry Keywords
Clinical ExperienceOncology IndustrySubject Matter ExpertExternal Partnerships
About the role
Key responsibilities & impact- Design, execute, and scale clinical development programs for precision oncology diagnostics
- Ensure alignment with real-world clinical decision-making and guideline development
- Define diagnostic-focused study priorities and oversee study execution
- Serve as a subject matter expert and lead working groups for oncology studies
- Establish external partnerships for high-quality study execution
- Lead scientific communication and evidence dissemination
- Support regulatory strategy and compliance
Requirements
What you’ll need- Master’s degree in Certified Genetic Counseling
- 5 or more years of clinical experience in academia or oncology industry
- 3 or more years of experience in clinical development, clinical utility studies, and/or real-world evidence generation.
Benefits
Comp & perks- Medical
- Dental
- Vision
- Life
- STD/LTD
- 401(k)
- Paid Time Off (PTO) or Flexible Time Off (FTO)
- Tuition Reimbursement
- Employee Stock Purchase Plan