Associate Director, Real World Evidence Strategy (Integrated Evidence Planning) (FSP Sponsor Dedicated)

Associate Director role supporting the development and maintenance of Integrated Evidence Plans within the Chief Medical Office. The position coordinates cross-functional evidence strategy execution, tracks plan implementation, and ensures alignment across medical affairs, regulatory, and clinical development functions.

Responsibilities

• Coordinate development of Integrated Evidence Plans based on established evidence strategy and asset priorities
• Facilitate cross-functional working sessions with Medical Affairs, Regulatory, Safety, and other partner functions to gather and reconcile input
• Monitor ongoing IEP activities including milestones, dependencies, risks, and changes to planned evidence-generation activities
• Prepare consolidated progress updates and decision-support materials for Therapeutic Area Leads and stakeholder teams
• Identify opportunities to apply evidence-generation approaches and escalate unresolved strategic questions to appropriate decision owners

Requirements

• PhD or Master's degree in Epidemiology preferred; MD, PharmD, or Bachelor's with substantial relevant experience
• Demonstrated experience with Integrated Evidence Planning coordination and execution
• Track record coordinating multi-stakeholder planning activities and translating strategy into actionable plans
• Strong understanding of drug development, medical evidence generation across asset lifecycle, and observational research methods
• Ability to facilitate cross-functional discussions, synthesize inputs, and escalate issues appropriately
• Strong organizational and project coordination skills with attention to dependencies and risk management
• Experience in matrix environments working with senior strategy and functional leaders