Clinical Development Scientist, Senior Manager

Role: Senior Manager, Clinical Development Scientist overseeing clinical trials in Internal Medicine. Primary objectives include ensuring scientific integrity, data quality, and compliance across studies, with potential supervisory responsibilities. Responsibilities encompass clinical support, protocol input, safety and data review, regulatory document contributions, site selection, investigator interface, and audit preparedness. Requirements: PhD/PharmD with 1+ year, or MA/MS with 5+ years, or BA/BS with 6+ years of clinical research experience; biopharma industry background. Preferred: cardiometabolic disease expertise, experience in study design, regulatory submissions, and scientific publication record. High-value: involvement in clinical phases, GxP compliance, data review, safety monitoring, and regulatory interactions within internal medicine. Work setup: hybrid role based in the U.S., with global travel possible. Emphasizes leadership, collaboration, and mentoring capabilities.