Co-own Tiny Health's clinical evidence roadmap and define study objectives aligned with product and regulatory goals.
Lead the design and publication of observational, interventional, and real-world evidence studies, including protocol development and statistical analysis plans.
Partner with cross-functional teams to ensure analytical rigor, translate findings into defensible claims, and present results to internal and external audiences.
Tiny Health advances lifelong health through precision microbiome science, addressing chronic disease from the first 1,000 days to the last. Founded in 2020 by microbiome scientists and physicians, the company is a remote-first team of about 30-50 employees with a culture of high standards, transparency, and continuous learning.
Lead medical work across sponsor-direct trials, including encoding new trials, iterating screening rules with engineering, and supervising a small medical contractor team.
Perform hands-on EMR review and clinical reasoning while setting strategic medical direction and contributing to customer and business conversations.
Partner with engineering to refine automated EMR screening, defining clinical logic for patient exclusion and human review, and contribute to product and trial design.
HealthMatch is on a mission to advance medicine by connecting patients with clinical trials. With over 2 million patients in our database and a growing trial portfolio, we are closing the gap in trial recruitment through technology and patient engagement.
Provide strategic vision for the clinical research team and generate rigorous evidence to inform Virta's care model and build credibility.
Oversee real-world evidence generation from claims and clinical datasets to demonstrate program impact and drive commercial growth.
Build KOL networks, communicate science, and partner with marketing to translate outcomes into compelling market narratives.
Virta Health is on a mission to reverse metabolic disease in one billion people through innovations in technology, personalized nutrition, and virtual care. The company has raised over $350 million from top-tier investors and partners with the largest health plans and employers.
Develop and execute the HEOR strategy for Braeburn’s product(s), ensuring alignment with medical, brand, and market access objectives.
Design, lead, and manage HEOR studies including retrospective database analyses, real-world evidence, patient-reported outcomes, and economic models.
Manage external vendors, oversee budgets and timelines, and disseminate evidence through peer-reviewed publications and scientific congress presentations.
We are dedicated to delivering solutions for people living with the serious consequences of opioid use disorder. We challenge the status quo, value authenticity, and strive to amplify all voices, empowering everyone to be successful.
Lead peer-reviewed and white-paper publications, turning complex clinical and claims data into evidence of Vida's impact for commercial growth and payer strategy.
Design and execute health-outcomes analyses using biometric, claims, and clinical data, applying advanced methods like multilevel modeling and survival analysis.
Partner with growth, strategy, and clinical teams to generate economic and clinical evidence supporting enterprise sales, client retention, and value-based care contracting.
Vida is a virtual, personalized obesity care provider using evidence-based treatment to help patients manage obesity and related conditions. It is trusted by Fortune 100 companies and aims to break down barriers to healthcare access through advanced technology and top-notch providers.
Identify and develop relationships with key decision makers in academic and community clinics, hospital systems, and payor organizations.
Educate and conduct meaningful scientific exchange with clinicians on the clinical attributes of Freenome products.
Stay abreast of the latest scientific and clinical advancements and represent the company at industry conferences.
Freenome is a biotechnology company developing blood-based cancer screening tests. The company is a growing organization dedicated to changing the landscape of cancer, with a collaborative and diverse culture.
Lead and mentor a team of Medical Science Liaisons in the East region, driving scientific engagement and medical strategy.
Oversee strategic planning and execution of field medical activities, including KOL relationship management and cross-functional collaboration.
Ensure compliance with regulatory standards and provide regular updates to Medical Affairs leadership.
Tarsus is a biopharmaceutical company focused on developing innovative treatments for eyecare. The company values commitment to patients, empowerment, and teamwork, and fosters a collaborative culture.
Lead clinical trial support services and site engagement strategy to maximize patient participation.
Orchestrate cross-functional teams to translate partner needs into scalable, data-driven programs.
Act as principal medical point of contact for pharma partners, driving contract negotiation and patient impact.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The Natera team consists of highly dedicated professionals from world-class institutions, who care deeply for our work and each other.
Drive clinical data market strategy and growth across enterprise customers.
Develop and execute the clinical data vision for enterprise sponsors.
Provide thought leadership and sales support to drive adoption of clinical data products.
Veeva Systems is a mission-driven cloud company that helps life sciences companies bring therapies to patients faster. It surpassed $3B in revenue and is a public benefit corporation with a culture of flexibility and employee success.
Lead market research and insight generation initiatives for the launch of envudeucitinib in psoriasis.
Act as a strategic advisor to brand and commercial leadership, integrating insights to drive commercial potential.
Execute robust market research plans, ensure high-quality insights, and collaborate cross-functionally.
Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. They are a hard-working, collaborative team on a mission to transform patients' lives.
Develop scientific materials such as slide decks, infographics, and social media posts to support medical affairs strategy.
Translate clinical and health economic evidence into clear, compliant content for internal and external stakeholders.
Coordinate with cross-functional teams and external vendors to deliver high-quality materials on time.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines for hypertension and related comorbidities like chronic kidney disease and sleep apnea. It is headquartered in Radnor, Pennsylvania, operates as a fully remote company, and fosters a diverse and dynamic team culture.
Lead clinical trial strategies and evidence-generation initiatives for diagnostic product development and regulatory submissions.
Serve as a scientific expert guiding study design, interpreting clinical data, and collaborating with stakeholders.
Ensure successful clinical programs across US and EU markets, ensuring scientific rigor and regulatory alignment.
The company develops innovative diagnostic solutions. They foster a collaborative environment emphasizing scientific excellence, continuous learning, and impactful solutions.
Lead and execute quantitative and mixed-methods real-world evidence and HEOR studies, including protocol development and statistical analysis.
Drive business development by generating new opportunities and managing client relationships in life sciences.
Provide strategic advisory on evidence generation to support value demonstration and clinical decision-making.
Avalere Health is a healthcare advisory firm dedicated to ensuring every patient is identified, treated, supported, and cared for. The company has global offices and a culture focused on diversity, inclusion, and flexible working.