
Medical Director
Posted Oct 20

Posted Oct 20
This is a fully remote position, open to applicants in North Carolina.
• Act as a primary medical resource specializing in precision medicine and cancer genomics.
• Collaborate closely with oncologists, clinicians, data scientists, epidemiologists, software engineers, product managers, account directors, and clinical data specialists.
• Contribute to the development, commercialization, and delivery of oncology research data and services utilizing tools such as artificial intelligence.
• Assist biopharma clients in applying clinical and molecular use cases throughout the entire R&D lifecycle.
• Facilitate custom data requests related to oncologic diseases, rare tumor types, and intricate multi-omic biomarker profiles.
• Define, design, and clinically validate bespoke datasets and analyses.
• Aid in target discovery, biomarker-based cohort characterization, tumor biology assessment, and combination therapy strategies.
• Support clients in leveraging real-world data for external control arms, historical cohorts, and synthetic control designs.
• Offer clinical and molecular data expertise during pre-sales, client scoping, and solution development.
• Convert clinical development planning and complex inclusion/exclusion criteria into precise data specifications.
• Collaborate with matrixed project teams on intricate dataset deliveries and tailored client requests.
• Create internal training materials and clinical documentation.
• Engage in research initiatives and present or speak at scientific conferences.
• MD (or equivalent) with a solid foundation in oncology, hematology, or a related subspecialty.
• Post-training clinical, academic, or early industry experience following the completion of a subspecialty fellowship.
• 1–3 years of experience for the Associate Medical Director level.
• 3–5+ years of experience for the Medical Director level.
• Familiarity with clinical trial design, protocol development, or early-phase (Phase I/II) clinical development.
• Exposure to laboratory translational oncology, cancer genomics, or biomarker discovery research is highly valued.
• Strong clinical intuition and comfort working with a range of low-incidence rare tumors and complex molecular landscapes.
• Ability to thrive in a matrix-structured environment with multiple stakeholders and product lines.
• Capacity to translate technical medical and genomic concepts for non-clinical internal teams.
• Proven ability to manage multiple tasks simultaneously and meet ongoing deadlines in a fast-paced, technology-driven environment.
• Demonstrated leadership, exceptional problem-solving, analytical, communication, multitasking, and prioritization skills.
• Enjoy work/life balance through flexible working hours and paid time off options.
• Receive a comprehensive compensation package.
• Participate in a 401(k) contribution plan.
• Access financial health resources, including one-on-one financial advice.
• Utilize mental well-being tools and services.
• Benefit from parental policies and support for family-building care and generous leave.
• Access programs supporting fertility, adoption, and surrogacy through a path to parenthood initiative.
• Receive travel support for safe healthcare services.
• Enjoy continuous learning opportunities.
• Participate in inclusion and belonging initiatives.
AbbVie
AbbVie
Pfizer
Pfizer
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