PV Risk Management Specialist
Baxter · Deerfield, IL
SafetyFull-time$112k–$154kCompany career page
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Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
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