
Scientific Director – Breast Cancer Portfolio
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in United States.
• Provide scientific and strategic direction for evidence generation across the breast cancer diagnostic product portfolio.
• Develop and implement integrated evidence-generation strategies for both in-development and commercially available assays.
• Establish evidence requirements for product development, regulatory submissions, reimbursement, clinical adoption, and guideline inclusion.
• Identify opportunities for indication expansion and the development of next-generation products.
• Collaborate with stakeholders to identify, assess, and prioritize clinical datasets.
• Provide scientific oversight for retrospective, prospective, observational, and translational studies.
• Create study concepts, research plans, protocols, and endpoints in conjunction with Biostatistics and Medical teams.
• Oversee study execution, interpretation, reporting, progress, and address scientific or operational challenges.
• Establish and nurture relationships with key opinion leaders, academic medical centers, cooperative groups, and research networks.
• Lead external scientific collaborations and act as the primary scientific contact for investigators.
• Write and review research proposals and assess external proposals.
• Develop publication strategies and spearhead abstracts, presentations, posters, and peer-reviewed manuscripts.
• Convert study findings into robust, clinically relevant evidence and present scientific data effectively.
• Collaborate with Product, Medical, Biostatistics, AI, and Market Access teams.
• Represent Clinical Development on cross-functional product teams and contribute to product claims, target product profiles, and commercialization strategies.
• Ph.D., M.D., Pharm.D., or an equivalent advanced degree in oncology, cancer biology, pathology, molecular biology, epidemiology, or a related field.
• A minimum of 5 years of experience in oncology clinical development, translational research, diagnostics, biotechnology, or pharmaceutical development.
• Proven expertise in breast cancer biology and clinical management.
• Experience in developing and executing clinical studies that support molecular diagnostics, digital pathology, genomic assays, AI-based diagnostics, or companion diagnostics.
• Background in leading collaborations with academic investigators and cooperative research groups.
• A track record of first-author, senior-author, or collaborative peer-reviewed publications.
• Experience in authoring study protocols, research proposals, abstracts, and manuscripts.
• Strong understanding of clinical trial methodology, observational studies, and translational research.
• Experience in cross-functional environments involving regulatory, product, commercial, and scientific stakeholders.
• Exceptional communication, presentation, and relationship-building skills, with the ability to engage clinical experts.
• Strong strategic thinking and analytical capabilities.
• Comfortable working independently in a fast-paced, collaborative startup environment with a high degree of ownership.
• Passion for enhancing patient care through AI-driven healthcare innovation.
• Expected travel of up to 5% domestically and internationally for scientific collaboration meetings.
• Preferred: experience in developing evidence strategies for commercially available diagnostic assays.
• Preferred: experience in supporting regulatory submissions for diagnostic products.
• Preferred: familiarity with breast cancer prognostic, predictive, and treatment-selection assays.
• Preferred: experience with real-world data, real-world evidence, and outcomes research.
• Preferred: knowledge of digital pathology, artificial intelligence, machine learning, or multimodal biomarkers.
• Preferred: existing relationships with breast cancer investigators, cooperative groups, and academic research networks.
• Equity is a fundamental part of the compensation package.
• 401k matching.
• Unlimited paid time off (PTO).
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