I provide expert tailored health services and epidemiology consulting to biotechnology companies, non-profits, and academics to help them achieve their mission and bring products to market.
Study Design and Implementation
Strategic guidance on designing and conducting population-based studies (cohort, case-control, case-cohort, randomized controlled trials), with expertise in pragmatic trials within real-world healthcare settings.
Protocol development, evaluation, refinement, and implementation
Endpoints and outcome measures
Multilevel factors that may influence outcomes and implementation
Data collection instruments and procedures
Study conduct, data quality assurance, and safety
Real-World Evidence (RWE) Generation
Strategic consultation on developing and executing RWE studies specializing in cancer screening and diagnostic technologies.
Evaluate design, location, and implementation strategies
Data source identification and feasibility assessment
Collaborate with data scientists and IT experts on using electronic health records, claims data, and patient registries
Scientific Communication and Collaboration
Developing communication strategies to effectively disseminate and implement scientific findings.
Peer-reviewed publications and conference presentations
Scientific reports and white papers
Collaborative partnerships with academic institutions, healthcare providers, and patient advocacy groups