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.