PV Risk Management Specialist Job at Baxter, Deerfield, IL

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  • Baxter
  • Deerfield, IL

Job Description

Baxter seeks a Pharmacovigilance Risk Management Specialist to author and maintain risk management plans supporting safe use of pharmaceutical products globally. The role involves leading cross-functional collaboration, ensuring regulatory compliance, and managing risk minimization strategies across multiple markets.

Responsibilities

  • Author and maintain Pharmacovigilance Risk Management Plans using global, regional, and local templates
  • Lead cross-functional review, feedback, and approval processes for PV-RMP submissions
  • Respond to regulatory authority questions and manage health authority commitments
  • Independently manage project timelines, deliverables, and submission activities
  • Partner with country affiliates and global stakeholders on risk management strategy implementation

Requirements

  • Bachelor's degree in Nursing, Biological Sciences, Medical, Clinical, or related field
  • Minimum two years pharmaceutical industry experience in Pharmacovigilance or Medical Affairs
  • Two to three years authoring Pharmacovigilance Risk Management Plans
  • Knowledge of EU pharmacovigilance requirements and global PV-RMP regulations
  • Strong analytical, critical thinking, and project management capabilities
  • Excellent written and verbal communication with cross-functional facilitation ability
  • Scientific or clinical knowledge with technical writing expertise

Compensation: $112,000 - $154,000 base annually

Job Tags

Local area

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