Associate Director, Global Clinical Safety Scientist

Role: Associate Director, Global Clinical Safety Scientist supporting global pharmacovigilance for Madrigal's MASH therapeutics, including Rezdiffra. Responsibilities: serve as safety lead for assigned projects; coordinate safety activities, contribute to safety document authoring/review (protocols, ICFs, Investigator’s Brochures); analyze and summarize clinical safety data to support regulatory submissions and internal review committees; collaborate on safety signal detection and assessment; contribute to safety sections of INDs, NDAs, and MAAs; prepare safety review materials and respond to safety inquiries; work closely with CSPV physicians and cross-functional teams. Requirements: minimum 10 years in clinical safety or pharmacovigilance within pharma/biotech; strong understanding of global safety regulations; experience with safety data analysis, regulatory safety reporting, and safety databases (Argus preferred); excellent communication and analytical skills; bachelor’s degree in a relevant scientific field; advanced degrees (PharmD, PhD, NP/PA, Master’s) preferred. High-Value: focus on metabolic diseases, specifically MASH, with involvement in Phase 3 outcomes trials. Work setup involves up to 10% travel. The role is integral to the pharmacovigilance function supporting a marketed drug and ongoing clinical trials.