Senior Director, Real World Evidence (Center of Excellence Lead)

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Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrine diseases. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and robust pipeline across preclinical and clinical development. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Come join our team as we transform the lives of others. Position Summary: The Senior Director, Real-World Evidence leads the Real-World Evidence Center of Excellence (RWE COE) within HEOR/RWE, serving as the technical execution engine that designs, conducts, and delivers real-world studies across the Crinetics portfolio. Working from evidence priorities defined by HEOR Therapeutic Area Leads and the Vice President, HEOR/RWE, the role directs a team of RWE Scientists to execute observational studies, claims and EHR analyses, registry analytics, external control arms, comparative effectiveness studies, drug utilization studies, and burden-of-illness research. The role sets technical and methodological standards for the function, builds enterprise real-world data infrastructure in partnership with IT and Commercial, and leads the RWE module of CrinRADAR. Reporting to the Vice President, HEOR/RWE, the Senior Director partners closely with HEOR Therapeutic Area Leads, Medical Affairs, Clinical Development, Biometrics, Patient Advocacy, Market Access, and external academic and data partners. Essential Job Functions and Responsibilities: These may include but are not limited to: Lead the delivery of the real-world evidence program across the portfolio, translating evidence priorities into rigorous, well-designed real-world studies. Provide leadership, career management, coaching, and mentoring to a team of RWE Scientists; recruit and develop talent and align team capacity to portfolio demand. Drive team objectives, prioritization, and resource allocation across competing therapeutic area needs. Operate across long-range lifecycle planning and near-term execution horizons. Design and oversee burden-of-illness, natural history, patient journey, drug utilization, external control arm, comparative effectiveness, and HTA-supportive real-world studies. Contribute to the design and operationalization of Crinetics-sponsored registries and lead registry-related analytics and evidence generation. Lead analyses using large healthcare databases and primary real-world data collection methods. Establish methodological standards, protocol templates, statistical analysis frameworks, and quality benchmarks. Conduct and supervise feasibility assessments, database selection, and study-design innovation. Partner with IT and Commercial to shape enterprise real-world data sourcing and analytics infrastructure. Lead the RWE module of CrinRADAR, supporting scalable and automated evidence generation. Establish data governance, contracting, and vendor management standards for real-world data assets. Partner with HEOR Therapeutic Area Leads to translate franchise-level evidence questions into executable plans. Contribute evidence to integrated evidence plans, value dossiers, and HTA submissions. Collaborate cross-functionally with Clinical Development, Biometrics, Regulatory, and Patient Advocacy. Build and steward external partnerships with academic investigators, data providers, and analytics vendors. Lead publication strategy and external scientific communication for the real-world evidence program. Represent Crinetics at scientific congresses and remain current with evolving real-world evidence methodologies and guidance. Ensure compliance with corporate policies and applicable healthcare laws and regulations. Other duties as assigned. Education and Experience: Required: Advanced degree in epidemiology, biostatistics, health services research, health economics, or related discipline (PhD, MD, PharmD, MPH, MSc). Minimum of 13 years of relevant pharmaceutical, biotechnology, or HEOR consulting experience. Minimum of 10 years supervisory years of experience. Demonstrated expertise in designing and executing observational studies using large real-world datasets across the product lifecycle. Experience leading center-of-excellence or function-level real-world evidence programs across multiple assets. Experience building and managing external real-world data vendor partnerships. Working knowledge of regulatory and HTA evidence requirements. Experience delivering real-world evidence into value dossiers and HTA submissions. Strong analytical, quantitative, and methodological expertise. Excellent communication and interpersonal skills with the abi

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