
501 - 1000 employees
Founded 2009
🏥 Healthcare
🧬 Biotechnology
⚕️ Healthcare Insurance
đź’° $125M Post-IPO Debt on 2022-09
Healthcare • Biotechnology • Healthcare Insurance
Adaptive Biotechnologies Corp. is a leader in immune-driven medicine, aiming to revolutionize disease detection and treatment. By utilizing the adaptive immune system, the company develops diagnostic and therapeutic solutions powered by its innovative Immune Medicine platform. They offer clinical diagnostics, particularly in Minimal Residual Disease (MRD) testing, and engage in drug discovery and therapeutic development through adaptive immunosequencing technologies. Their biopharma services support the progression of clinical trials and the development of transformative medicines. Adaptive Biotechnologies leverages the complex biology of the immune system, decoding it to advance medical science and improve patient outcomes.
🔥 12 hours ago
🇺🇸 United States – Remote
đź’µ $206.4k - $309.6k / year
⏰ Full Time
đź”´ Lead
👨‍⚕️ Medical Director
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501 - 1000 employees
Founded 2009
🏥 Healthcare
🧬 Biotechnology
⚕️ Healthcare Insurance
đź’° $125M Post-IPO Debt on 2022-09
Healthcare • Biotechnology • Healthcare Insurance
Adaptive Biotechnologies Corp. is a leader in immune-driven medicine, aiming to revolutionize disease detection and treatment. By utilizing the adaptive immune system, the company develops diagnostic and therapeutic solutions powered by its innovative Immune Medicine platform. They offer clinical diagnostics, particularly in Minimal Residual Disease (MRD) testing, and engage in drug discovery and therapeutic development through adaptive immunosequencing technologies. Their biopharma services support the progression of clinical trials and the development of transformative medicines. Adaptive Biotechnologies leverages the complex biology of the immune system, decoding it to advance medical science and improve patient outcomes.
• Lead the medical aspects of the autoimmune program and create and execute the clinical development and evidence plan • Provide disease-area, physician, and patient input to R&D, Product, Commercial, and Market Access teams • Design and oversee clinical validation, clinical utility, real-world evidence, and early clinical experience programs • Develop and review protocols, investigator materials, clinical study reports, regulatory documents, publications, and presentations • Interpret results and recommend next steps to program teams • Develop KOL and investigator relationships, lead advisory activities, and cultivate scientific collaborations and investigator-initiated research • Partner with Biopharma Business Development to integrate Adaptive assays into drug-development programs • Monitor the evolving autoimmune disease landscape to evaluate unmet needs and inform product strategy • Build internal autoimmune expertise and represent Adaptive at scientific meetings and with external stakeholders • Define medical resourcing plans and recruit, manage, and develop the team as the program grows • Manage assigned budgets, vendors, timelines, and compliance requirements • Lead clinical strategy across the product lifecycle from early discovery through commercialization • Perform all other duties as assigned
• MD or DO degree from an accredited institution • Medical license in good standing (preferred) or documented prior licensure in good standing • 8+ years of experience • At least 4 years of post-training clinical, translational, or clinical-research experience in autoimmune or immune-mediated disease • At least 4 years of industry experience in clinical development, medical affairs, diagnostics, biotechnology, or biopharma, including work with molecular diagnostics, biomarkers, or precision-medicine products • Board certification or eligibility in a specialty that manages autoimmune disease • Experience developing and executing clinical evidence plans and prospective studies, including protocols, data interpretation, study reports, and scientific publications or presentations • Working knowledge of diagnostic clinical-performance and clinical-utility study design, biostatistics, GCP, human-subject protections, and applicable FDA, CLIA/CAP, privacy, and quality requirements • Track record of partnering across R&D, Regulatory, Quality, Biostatistics, Product, Commercial, Market Access, and Business Development • Experience developing KOL and investigator relationships and leading advisory boards or scientific collaborations • Strong scientific writing and presentation skills • Ability to travel up to 25% • Not currently sponsoring candidates requiring work authorization support for this position
• Equity grant • Bonus eligible • Remote work from home • Travel up to 25% • Adaptive benefits program (benefits-at-a-glance) • Diverse, equitable, and inclusive workplace
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