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Freenome

Director, Evidence Generation and Publications

Freenome
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remote senior full-time $214,625 - $305,550

First indexed 24 Jul 2026

Description

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.

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 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 GPP and ICMJE.
  • Maintain high standards for scientific integrity, authorship, transparency, and data accuracy.
  • Manage vendors, research partners, contracts, budgets, timelines, and program risks.

Requirements

  • Advanced degree (MS or PhD) in medicine, science, public health, epidemiology, health economics, pharmacy, or a related field.
  • 10+ years of relevant diagnostics, medical device, or healthcare experience, ideally in oncology.
  • Demonstrated experience leading evidence generation and publication strategies.
  • Strong knowledge of clinical research, real-world evidence, epidemiology, biostatistics, and scientific data interpretation.
  • Experience authoring and supervising manuscripts, abstracts, posters, and scientific presentations.
  • Proven ability to lead complex cross-functional initiatives in a matrixed organization.
  • Excellent written, verbal, presentation, and stakeholder-management skills.
  • Strong commitment to scientific integrity and compliant collaboration.

Nice to haves

  • Experience in oncology, cancer screening, molecular diagnostics, genomics, multiomics, or liquid biopsy.
  • Experience supporting diagnostic products, including screening tests, through their development, regulatory review, launch, and/or lifecycle management.
  • Experience with real-world data, health economics, implementation science, or healthcare delivery research.
  • Established relationships with investigators, academic institutions, or professional societies.
  • Prior people-management experience.

Benefits

  • The US target range of our base salary rate for new hires is $214,625 - $305,550.
  • You will also be eligible to receive equity, cash bonuses, and a full range of medical, financial, and other benefits depending on the position offered.
This listing is enriched and indexed by YubHub. To apply, use the employer's original posting: https://job-boards.greenhouse.io/freenome/jobs/8645988002