Associate Medical Director

Role: Medical Safety Review (MSR) lead focusing on clinical trial Serious Adverse Events (SAEs) within AbbVie's immunology, oncology, and neuroscience therapeutic areas. Primary objectives include conducting causality assessments, developing company safety analyses (SUSARs), and providing therapeutic area leadership. Responsibilities encompass medical review of SAEs, communication with trial stakeholders, contributing to global safety processes, and supporting audits and training. May have people management duties with direct reports. Requirements: MD or equivalent; 1-2 years drug safety experience with medical assessment/clinical case review for Associate Medical Director II; leadership experience preferred. High-Value: clinical safety in immunology, oncology, or neuroscience, post-marketing and clinical trial phases, SUSAR development, global regulatory compliance, GxP adherence, and cross-functional safety collaboration. WorkSetup: not specified; potential for international or remote work based on location.