data analysisartificial intelligenceoncologyclinical trialsreal world evidenceprecision medicinecancer genomicsbiomarker discovery
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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В Company hidden хорошо очерченная специализированная роль на стыке онкологии, прецизионной медицины и реальных клинических данных, но без зарплатного диапазона сложнее оценить компенсацию.
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Зарплата не указанаЧёткие задачиНа стыке медицины и данныхГибкие условия
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Текст:
Hirify AI/Оригинал
TL;DR
Medical Director (Precision Medicine): Developing and delivering oncology research data and services for biopharma clients with an accent on precision medicine, cancer genomics, and real-world evidence. Focus on translating clinical and molecular data into target discovery, biomarker-defined cohorts, trial designs, external control arms, and custom datasets.
Location: Remote - US; align working hours with the team. hirify.global also lists offices in New York, NY and Durham.
Company
hirify.global develops oncology research data and services to support real-world evidence and a more connected cancer-care ecosystem.
What you will do
Provide clinical oncology and precision medicine expertise for high-volume custom data requests across oncologic diseases, rare tumors, and complex multi-omic biomarker profiles.
Partner with biopharma clients on target discovery, biomarker-defined cohorts, tumor biology, combination therapy strategies, and reverse translation of clinical trial findings.
Apply clinical development and trial design principles to real-world evidence, including external control arms, historical cohorts, and synthetic control designs.
Support pre-sales, client scoping, and solution development by translating clinical development plans and complex inclusion/exclusion criteria into data specifications.
Collaborate with oncologists, clinicians, data scientists, epidemiologists, software engineers, product managers, account directors, and clinical data specialists on custom data solutions.
Build internal training and clinical documentation, contribute to research studies, and present or speak at scientific conferences.
Requirements
MD or equivalent with foundational training in oncology, hematology, or a related subspecialty.
Oncology experience after subspecialty fellowship, with 1–3 years for Associate Medical Director or 3–5+ years for Medical Director.
Direct experience with cancer genomics.
Clinical, academic, or early industry experience after training.
Familiarity with clinical trial design, protocol development, or early-phase Phase I/II clinical development.
Deep clinical intuition and the ability to work across diverse low-incidence rare tumors and complex molecular landscapes.
Ability to collaborate in a matrix-structured environment and explain technical medical and genomic concepts to non-clinical teams.
Leadership, problem-solving, analytical, communication, multitasking, prioritization, and operational execution skills in a fast-paced technology-driven environment.
Nice to have
Exposure to laboratory translational oncology, cancer genomics, or biomarker discovery research.
Experience with precision medicine ownership at a scope appropriate for the Associate Medical Director or Medical Director level.
Culture & Benefits
Flexible work hours and flexible paid time off.
Comprehensive compensation package.
401(k) contributions and financial health resources, including one-to-one financial advice.
Mental well-being tools and services.
Parental benefits, family-building care, fertility, adoption, surrogacy support, and generous leave.
Travel support for safe healthcare services and resources supporting continuous learning, inclusion, and belonging.
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