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Freenome is seeking a Director of Evidence Generation and Publications to lead integrated evidence-generation and publication strategies across the company's portfolio. This role will identify evidence gaps, develop research and analysis plans, and oversee the dissemination of clinical, real-world, economic, and operational data.
Key responsibilities include:
Evidence-generation strategy: Develop and execute integrated evidence plans aligned with clinical, regulatory, market-access, and commercial priorities. Identify evidence gaps and translate them into executable research questions, study concepts, and analysis plans. Lead post hoc analyses, real-world evidence and registry studies, and investigator-sponsored research. Guide evidence development throughout the product lifecycle (feasibility, validation, and post-marketing studies). Establish clear governance, prioritization, timelines, and measures of impact.
Publication and scientific-dissemination strategy: Develop and manage publication plans aligned with Freenome's scientific communication strategy. Oversee manuscripts, abstracts, posters, oral presentations, and other scientific materials. Ensure timely, accurate, and compliant dissemination of data. Partner with internal authors, external investigators, medical writers, statisticians, and third-party vendors. Track publication progress and scientific impact.
Scientific leadership and cross-functional collaboration: Serve as a strategic partner across Science, Scientific and Medical Affairs, Clinical, Regulatory, Market Access, Commercial, and Biometrics. Translate complex findings into clear and credible scientific narratives. Provide guidance on study design, endpoints, analyses, interpretation, and dissemination. Align internal teams on evidence priorities, scientific messaging, and publication timing. Present strategies and program updates to senior leadership.
External research and scientific engagement: Represent Freenome at scientific congresses, advisory boards, and research meetings. Build relationships with investigators, academic institutions, and healthcare systems. Evaluate and support investigator-sponsored research. Identify external partnerships that strengthen Freenome's evidence base.
Governance, quality, and compliance: Ensure adherence to applicable company policies, publication standards, and ethical guidelines, including Good Publication Practice (GPP) and International Committee of Medical Journal Editors (ICMJE) standards.
This role reports to the VP of Medical Affairs and requires deep experience in evidence generation, publication planning, and cross-functional collaboration in a biotech or healthcare setting.
