Director, Evidence Generation and Publications

Freenome

Director leading integrated evidence-generation and publication strategies across Freenome's portfolio. Partnering across multiple departments to oversee clinical and operational data dissemination.

Posted 7/24/2026full-timeRemote • 🇺🇸 United StatesLead💰 $214,625 - $305,550 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in evidence generation, publication strategy, and clinical research, with a strong focus on oncology and real-world evidence. Proven ability to lead cross-functional initiatives and communicate complex scientific findings effectively.

Highest-signal resume keywords

Evidence GenerationPublication StrategyClinical ResearchReal-World EvidenceOncology Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

BiostatisticsEpidemiologyScientific Data InterpretationStudy DesignAnalysis PlansResearch Question DevelopmentPost Hoc AnalysesRegulatory ReviewHealth EconomicsImplementation Science

Soft Skills

Stakeholder ManagementExcellent Written CommunicationPresentation SkillsVerbal CommunicationCollaboration

Certifications & Qualifications

Advanced Degree (MS or PhD)

Industry Keywords

DiagnosticsMedical DeviceHealthcareOncologyCancer ScreeningMolecular DiagnosticsGenomicsMultiomicsLiquid BiopsyHealthcare Delivery Research

About the role

Key responsibilities & impact

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.
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.
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.
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.

Requirements

What you’ll need

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

Comp & perks

You will also be eligible to receive equity
cash bonuses
a full range of medical, financial, and other benefits depending on the position offered