Medical Director

Posted 5 days ago

This is a fully remote position, open to applicants in New York, +1 more state.

πŸ“‹ Description

β€’ Act as a primary medical resource specializing in precision medicine and cancer genomics.

β€’ Assist in the development, commercialization, and provision of oncology research data and services using artificial intelligence and other methodologies.

β€’ Support biopharma clients in implementing clinical and molecular use cases throughout the entire R&D lifecycle.

β€’ Define the scope, design, and clinically validate tailored datasets and analyses for oncological diseases.

β€’ Aid in target discovery, characterization of biomarker-defined cohorts, evaluation of tumor biology, and strategies for combination therapies.

β€’ Guide clients in utilizing real-world data for external control arms, historical cohorts, and synthetic control designs.

β€’ Offer expertise in clinical and molecular data during pre-sales, client scoping, and solution development.

β€’ Convert clinical development planning, target validation, and inclusion/exclusion criteria into accurate data specifications.

β€’ Collaborate with matrixed project teams on intricate dataset deliveries and customized client requests.

β€’ Create internal training materials and clinical documentation.

β€’ Engage in research studies and present findings or speak at scientific conferences.

β€’ Work alongside oncologists, clinicians, data scientists, epidemiologists, software engineers, product managers, account directors, and clinical data specialists.


⛳️ Requirements

β€’ MD (or equivalent) with foundational training in oncology, hematology, or a related subspecialty.

β€’ Clinical, academic, or early industry experience post-training after completing a subspecialty fellowship.

β€’ 3-5+ years of experience for the Medical Director position; 1-3 years for the Associate Medical Director position.

β€’ Knowledge of clinical trial design, protocol development, or early-phase (Phase I/II) clinical development.

β€’ Valuable exposure to laboratory translational oncology, cancer genomics, or biomarker discovery research.

β€’ Strong clinical intuition and a willingness to learn about diverse low-incidence rare tumors and complex molecular landscapes.

β€’ Experience in a matrix-structured environment with various stakeholders and product lines.

β€’ Capability to convey technical medical and genomic concepts to non-clinical internal teams.

β€’ Proficient in managing multiple tasks simultaneously and meeting ongoing deadlines in a fast-paced, technology-driven setting.


🏝️ Benefits

β€’ Enjoy work/life flexibility through adaptable work hours and flexible paid time off.

β€’ Receive a comprehensive compensation package.

β€’ Benefit from a 401(k) contribution to assist you in achieving your retirement planning objectives.

β€’ Access financial health resources, including personalized financial advice.

β€’ Utilize mental well-being tools and services.

β€’ Take advantage of parental benefits and policies that include family-building care and generous leave.

β€’ Participate in programs supporting fertility, adoption, and surrogacy.

β€’ Get travel support for safe healthcare services.

β€’ Earn an annual bonus.

β€’ Share in equity opportunities.

β€’ Receive ongoing support for continuous learning.

β€’ Access resources promoting inclusion and belonging.

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