# Director, Evidence Generation and Publications

**Company**: Freenome
**Location**: Remote
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Salary**: $214,625 - $305,550
**Category**: Medical Affairs
**Industry**: Healthcare

**Apply**: https://job-boards.greenhouse.io/freenome/jobs/8645988002?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_3978c8e9-c1a

## 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.

## Skills

### Required
- evidence generation
- publication planning
- cross-functional collaboration
- clinical research
- real-world evidence
- epidemiology
- biostatistics
- scientific data interpretation
- manuscript writing
- scientific presentation

### Nice to have
- oncology
- cancer screening
- molecular diagnostics
- genomics
- multiomics
- liquid biopsy
- health economics
- implementation science
- healthcare delivery research

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Source: [Apply at job-boards.greenhouse.io](https://job-boards.greenhouse.io/freenome/jobs/8645988002?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)