
201 - 500 funcionários
Fundada em 2014
🏥 Saúde
🧬 Biotecnologia
🤖 Inteligência Artificial
💰 $290.000.000 Corporate Round em 2022-01
Healthcare • Biotechnology • Artificial Intelligence
A Freenome é uma empresa focada em avançar na detecção precoce do câncer através da integração de inovação científica e inteligência artificial. Sua plataforma utiliza tecnologia multiómica para identificar o câncer em seus estágios mais tratáveis, permitindo a intervenção precoce. A empresa enfatiza um método padrão de coleta de sangue para facilitar o uso, visando redefinir a triagem de câncer. A Freenome é impulsionada por um robusto programa de pesquisa clínica e está comprometida em descobrir, desenvolver e validar testes de detecção precoce de câncer, empregando uma equipe multidisciplinar dedicada a expandir os limites do que é possível em diagnóstico oncológico.
🕒 Julho 24
🇺🇸 Estados Unidos – Remoto (EUA)
💵 $214.625 - $305.550 / ano
⏰ Tempo Integral
🔴 Especialista
👔 Diretor
🦅 Patrocina Visto H1B
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

201 - 500 funcionários
Fundada em 2014
🏥 Saúde
🧬 Biotecnologia
🤖 Inteligência Artificial
💰 $290.000.000 Corporate Round em 2022-01
Healthcare • Biotechnology • Artificial Intelligence
A Freenome é uma empresa focada em avançar na detecção precoce do câncer através da integração de inovação científica e inteligência artificial. Sua plataforma utiliza tecnologia multiómica para identificar o câncer em seus estágios mais tratáveis, permitindo a intervenção precoce. A empresa enfatiza um método padrão de coleta de sangue para facilitar o uso, visando redefinir a triagem de câncer. A Freenome é impulsionada por um robusto programa de pesquisa clínica e está comprometida em descobrir, desenvolver e validar testes de detecção precoce de câncer, empregando uma equipe multidisciplinar dedicada a expandir os limites do que é possível em diagnóstico oncológico.
• 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.
• 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.
• You will also be eligible to receive equity • cash bonuses • a full range of medical, financial, and other benefits depending on the position offered
Candidatar-se🕒 Julho 24
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