Director, Evidence Generation and Publications

About this role

About this opportunity:

Freenome is seeking a Director, 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. The Director will partner across Scientific and Medical Affairs, Clinical Development, Biostatistics, Data Science, Regulatory Affairs and Market Access.

The ideal candidate is a strategic scientific leader with deep experience in evidence generation, publication planning, and cross-functional collaboration.

This role reports to the VP, Medical Affairs. This role will be a Remote role.

What you’ll do:

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 readily 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.

• 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 GPP and ICMJE.