Senior Medical Monitor

Key responsibilities: Provide medical oversight for clinical trials and observational studies, ensuring participant eligibility and safety Review and analyze adverse events and safety data, leading safety activities and participating in cross-functional meetings Guide the preparation of regulatory documents and safety reports, serving as a medical subject matter expert for project teamsRequired qualificationsMedical degree (MD, DO, or international equivalent) 5+ years of medical monitoring, clinical, or research experience Experience with protocol amendments and aggregate data review for clinical trials Excellent knowledge of medical terminology, clinical pharmacology, and regulatory guidelines (ICH, FDA, EMA) Strong scientific writing skills and proficiency with MS Office applications