Associate Director, Clinical Site Management and Monitoring Oversight

Role: Develop and lead Madrigal’s Clinical Monitoring Oversight program, including building and managing an internal US CRA field force for biopharma clinical trials. Responsibilities: oversee risk-based remote and on-site monitoring activities, manage relationships with CRO partners and trial sites, develop training and oversight processes, and monitor CRA performance and site engagement within the US. Qualifications: Bachelor’s in life sciences, 10+ years in clinical operations or monitoring, with 2+ years in CRA or Monitoring Oversight roles; experience managing CRAs and developing training systems; proficiency with Veeva Vault systems; ability to travel up to 50% within the US. High-value: focus on metabolic liver disease (MASH), Phase 3 and ongoing trials, with a strong emphasis on monitoring oversight, CRA team development, and cross-functional collaboration. Work setup: US-based role with travel; reports to Sr. Director of CRA Field Force.