Manager, REMS Operations

Role: Support FDA-mandated REMS programs within a biopharma setting, ensuring compliance, operational efficiency, and program oversight. Responsibilities: manage day-to-day REMS operations, coordinate governance activities, monitor program health, facilitate communication of modifications, and partner with cross-functional teams and external vendors. Requirements: 4-6 years pharma industry experience, 2+ years project/program management, proficiency in Microsoft Office, excellent communication, highly organized, Bachelor's degree in a relevant field. Preferred: REMS experience. High-Value: Regulatory compliance, REMS program management, cross-functional stakeholder engagement, documentation for audits and inspections. WorkSetup: Not specified; likely remote based on context.