Associate Medical Director (PS-MD)
Core
Lead Medical Safety Review (MSR) of clinical trial Serious Adverse Events (SAEs), including causality assessment and company analysis development, while providing therapeutic area leadership.
Role type
Associate Medical Director (Drug Safety)
Builds
Clinical safety reports and company analyses for AbbVie products and development compounds
Domain
Pharmaceutical drug safety and clinical trial management
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Medical review of clinical SAEs, causality assessment of adverse events, company analysis development for SUSARs, therapeutic area leadership, global safety regulations knowledge, disease state understanding
Preferred skills
None stated
Technologies
None stated
Responsibilities
Lead individual safety projects or initiatives, perform medical review of clinical SAEs, develop Company Analysis for SUSARs, communicate with clinical trial stakeholders, contribute to Global Patient Safety (GPS) initiatives and audits
Seniority
Associate, hands-on IC