Note: The job is a remote job and is open to candidates in USA. Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The Senior Director, Real-World Analytics & Programming will lead the establishment of analytics capabilities, working across departments to develop strategies and oversee key projects that leverage real-world data to enhance patient care.
Responsibilities
- Develop and lead real-world analytics and programming plans to support portfolio, Medical Affairs, HEOR/RWE, and epidemiology goals
- Provide subject matter expertise on RWD data sources, their strengths/limitations, and the feasibility of answering key scientific questions using available data
- Oversee high-quality RWE study design, protocol development, statistical analysis planning, and final reporting in support of regulatory submissions and product value evidence – typical projects include include systematic literature reviews, natural history studies, clinical trial design and optimization, comparative effectiveness and safety, and healthcare resource utilization types of studies, post-approval safety studies leveraging RWD, as well as RWD-related insights such as quick feasibility and information used to inform our fast-moving clinical programs
- Ensure fit-for-purpose methods are used to provide scientific rigor to non-interventional studies so that they adhere to global regulatory guidance frameworks and are acceptable to other key stakeholders
- Communicate insights and analysis effectively to senior stakeholders, regulatory agencies, payers, and scientific audiences through written reports and presentations
- Participate in governance, feasibility review, and multidisciplinary project teams, ensuring RWD analytics add meaningful insight at key decision points
- Build, mentor, and lead a high-performing analytics team with expertise in epidemiology, biostatistics, data science, and RWE methodologies
- Develop real-world analytics and programming standards that enhance consistency, and partner with other functions to establish data ingestion pipelines
Skills
- PhD / DSc / DrPH / MPH in epidemiology or biostatistics, or a relevant advanced science degree and at least 12 years of experience with real-world analytics and programming and evidence generation in pharma/biotech
- Demonstrated experience leading complex real-world analytics and programming projects from concept through delivery, including study design, analysis, and reporting/submission to regulatory agencies
- Strong expertise with RWD sources (claims, EHR, registries, -omics data, linked datasets) and analytic tools (R/SAS/Python)
- Demonstrated technical knowledge of epidemiologic, biostatistical, and data science methods
- Knowledge of drug and clinical development process for genomic/targeted medicines
- Excellent analytic and problem-solving skills
- Strong interpersonal skills and the ability to work effectively in multidisciplinary teams, including ability to provide oversight to vendors
- Experience in oncology real-world analytics and programming
- Track record of publications or presentations in real-world analytics and programming/epidemiology/data science
- Experience aligning RWE strategy to regulatory and payer evidence planning, especially around the planning and execution of post-approval safety studies
Benefits
- Competitive cash compensation
- Robust equity awards
- Strong benefits
- Significant learning and development opportunities
Company Overview
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