Director, Medical - Clinical Research Scientist

Role: Clinical Research Scientist (CRS) in Lilly's Cardiometabolic Research (CMR) Program, focusing on early-phase compounds, including those targeting women’s health. Responsibilities: design, oversee, and report on global Phase I and II clinical trials, support pre-clinical studies, collaborate with discovery and non-clinical research teams, ensure compliance with GCP and regulatory standards, and contribute to scientific data dissemination. Engage in protocol review, investigator selection, patient safety monitoring, and regulatory support activities. Collaborate externally with healthcare professionals, professional societies, and regulatory agencies for data exchange and business development. Requirements: PhD in Development Biology, Immunology, Cell Biology, Physiology, Pharmacology, or Neuroscience; 5+ years in clinical development; experience in pharmaceutical or clinical research preferred; strong communication and interpersonal skills; willingness to travel domestically and internationally. High-Value: Early-phase clinical development, women’s health, pharmacokinetics, biomarker development, regulatory interactions, and cross-functional teamwork. Work setup: Not specified; travel required.