Physician Researcher, Study Design, Registry

Responsibilities Lead the design of registries, observational studies, and pragmatic/real-world evidence (RWE) studies Serve as the primary clinical point of contact for external customers, investigators, sites, and partner organizations Partner with Clinical Operations, Biostatistics, Epidemiology, and Regulatory Affairs to ensure protocols meet scientific, regulatory, and operational standards Identify, cultivate, and lead strategic research partnerships with academic medical centers, health systems, professional societies, and external research networks Requirements M.D. or D.O. (or international equivalent) with active or eligible medical licensure 3–5 years of pharmaceutical, biotech, or CRO industry experience in clinical development, medical affairs, or real‑world evidence Strong understanding of epidemiological methods, biostatistics fundamentals, and real‑world data sources Working knowledge of GCP and regulatory requirements for observational research Excellent written/verbal communication skills across scientific and non‑scientific audiences Core Competencies Demonstrates expertise in leading the design and execution of registries and real-world evidence studies, with a strong foundation in epidemiological methods and biostatistics. Capable of fostering strategic partnerships and ensuring compliance with regulatory standards in clinical research. #J-18808-Ljbffr Jobtailor