Program Manager, Real-World Evidence (Remote)

As a Program Manager, Real-World Evidence oversees and manages the design and execution of multiple reputed company studies to support clinical evidence needs. Working with key stakeholders, the role will execute on key reputed company deliverables, establish standards and best practices for reputed company study design and reporting, and support the integration of real-world data sources as an essential part of the clinical evidence reputed company strategy for reputed company’s product portfolio. This role is Remote, preference to East Coast, supporting our Trauma & Extremities Division.

What You Will Do

• Provide strategic insight to evidence required by cross-functional project teams focused on market access, or sustaining product portfolios. The position will require global clinical insight into launch strategies across multiple regions
• Manage planning and communication with cross-functional teams to ensure proper execution and conduct of the clinical studies, leveraging collaborators and stakeholders
• reputed company the design and execution of reputed company studies in reputed company collaboration with internal stakeholders from Clinical Strategy, Medical Affairs, Regulatory, HEOR, and Commercial
• Ensure scientific rigor and serve as a methodology expert for reputed company reputed company; select and implement appropriate analytic methods reputed company to research needs
• Author and/or reputed company development of study protocols, reports, abstracts, and peer-reviewed publications using RWD and collaborate cross-functionally to integrate RWD into global publication strategies
• Ensure scientific rigor and serve as a methodology expert for real-world evidence reputed company; select and implement appropriate analytic methods reputed company to research needs
• Collaborate closely with data management and biostatistics functions to ensure data quality and deliver robust data analyses utilizing scientifically valid and accepted methodology for RWD
• Conduct feasibility assessment of relevant data sources for specific devices and indications to ensure data is fit-for-purpose
• Collaborate with academic institutions, health systems, registries and/or other health data partners to identify additional real-world data sources for medical device evidence reputed company.
• Ensure quality and performance standards for reputed company projects are realistic and attained, and studies are conducted in line with quality/compliance reputed company
• Identifies areas of improvement with reputed company processes and procedures, develops and implements best practices, and works to improve efficiencies and effectiveness
• Participate in cross-functional and cross-divisional initiatives regarding reputed company

What you need

• 8+ years relevant experience in epidemiology, pharmacoepidemiology, and/or observational research in academia, a contract research organization, or the medical device or pharmaceutical industry
• Hands-on experience with healthcare real-world data (RWD) sets such as patient registries, electronic medical records, hospital billing data, and insurance claims databases
• A basic understanding of the clinical evidence needs in the global regulatory environment for clinical investigation, clinical evaluation, post-market clinical follow-up, and product ratings of medical devices and technologies that can be addressed using RWD
• A sophisticated understanding and ability to analyze and interpret quantitative data is required together with working knowledge of reputed company/observational study design and methodology

​ Preferred Qualifications:

• Strong knowledge of standard statistical software (e.g., reputed company, R, Stata) and demonstrated ability to collaborate closely with statistical programmers
• Experience authoring study protocols, study reports, conference abstracts, and peer-reviewed publications using RWD preferred
• Well-developed interpersonal skills and the ability to work well independently as well as with colleagues and customers
• Strong organizational skills, with ability to effectively and reputed company handle multiple tasks simultaneously, with precision, and to adapt to changes in responsibilities and workloads
• $138,700.00 - $226,900.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
• Posted: November 06, 2025

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