Clinical Development Scientist, Senior Manager

Role: Senior Manager in Clinical Development overseeing clinical trials within Internal Medicine, responsible for scientific oversight, data integrity, and quality assurance. Key responsibilities include supporting protocol development, contributing to study design, safety monitoring, data review, and regulatory document preparation; managing external committees; and ensuring compliance with GxP and ICH/GCP standards. Qualifications: PhD, PharmD, or equivalent with at least 1 year (or MA/MS with 5+ years, BA/BS with 6+ years) clinical research experience in biopharma. Preferred: cardiometabolic disease expertise, study design and regulatory experience, scientific publication record, strong communication skills, leadership abilities, and knowledge of global regulatory landscapes. High-Value: focus on clinical studies in Internal Medicine, including safety management, data review, and protocol development; involvement in regulatory interactions and audits. Work setup: hybrid role based in the U.S., requiring ~2.5 days on-site weekly, with potential for global travel.