Associate Medical Director (PS-MD)

Role: Medical Safety Review (MSR) specialist focused on safety assessment of clinical trial Serious Adverse Events (SAEs) and causality analysis within AbbVie's therapeutic areas, primarily immunology, oncology, and neuroscience. Responsibilities: perform medical review of clinical SAEs, develop company analyses for Suspected Serious Adverse Reactions (SUSARs), communicate effectively with trial stakeholders, conduct causality assessments for post-marketing safety reports, and understand safety profiles of AbbVie products and related drugs. Contribute to global safety initiatives, support audits and inspections, and participate in MSR training activities. Requirements: MD or equivalent with 1–2 years drug safety experience involving medical assessment and clinical case review. HighValue: focus on pharmacovigilance within immunology, oncology, neuroscience; safety analysis of clinical trial and post-market data; regulatory compliance with global safety standards. WorkSetup: not specified, but position implies collaboration across global safety teams.