Director, Evidence Generation and Publications

This is a fully remote position, open to applicants in United States.

📋 Description

• Develop and implement integrated evidence plans that are in line with clinical, regulatory, market-access, and commercial objectives.

• Identify gaps in evidence and convert them into actionable research questions, study concepts, and analysis frameworks.

• Lead post hoc analyses, real-world evidence studies, registry studies, and research sponsored by investigators.

• Oversee evidence development throughout the entire product lifecycle, including feasibility, validation, and post-marketing studies.

• Establish clear governance, prioritization, timelines, and impact measurement criteria.

• Create and manage publication plans that align with Freenome’s scientific communication strategy.

• Supervise manuscripts, abstracts, posters, oral presentations, and other scientific documents.

• Ensure the timely, accurate, and compliant dissemination of data.

• Collaborate with internal authors, external investigators, medical writers, statisticians, and third-party vendors.

• Monitor publication progress and evaluate scientific impact.

• Act as a strategic partner across various departments including Science, Scientific and Medical Affairs, Clinical, Regulatory, Market Access, Commercial, and Biometrics.

• Convert 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 timelines.

• Present strategies and program updates to senior leadership.

• Represent Freenome at scientific congresses, advisory boards, and research meetings.

• Cultivate relationships with investigators, academic institutions, and healthcare systems.

• Assess and support research sponsored by investigators.

⛳️ Requirements

• Advanced degree (MS or PhD) in medicine, science, public health, epidemiology, health economics, pharmacy, or a related discipline.

• Over 10 years of relevant experience in diagnostics, medical devices, or healthcare, preferably in oncology.

• Proven experience in leading strategies for evidence generation and publication.

• Strong understanding of clinical research, real-world evidence, epidemiology, biostatistics, and the interpretation of scientific data.

• Experience in authoring and overseeing manuscripts, abstracts, posters, and scientific presentations.

• Demonstrated ability to lead complex cross-functional projects within a matrixed organization.

• Exceptional written, verbal, presentation, and stakeholder-management abilities.

• Strong dedication to scientific integrity and compliant collaboration.

• Nice to haves:

• Experience in oncology, cancer screening, molecular diagnostics, genomics, multiomics, or liquid biopsy.

• Experience in supporting diagnostic products, including screening tests, throughout their development, regulatory review, launch, and/or lifecycle management.

• Familiarity with real-world data, health economics, implementation science, or healthcare delivery research.

• Established networks with investigators, academic institutions, or professional societies.

• Previous experience in people management.

🏝️ Benefits

• You will also be eligible to receive equity.

• Cash bonuses.

• A comprehensive range of medical, financial, and other benefits depending on the position offered.