Pharmacovigilance Scientist - Remote

Overview

The Pharmacovigilance Scientist serves an integral role in safety data analyses for assigned investigational and/or marketed product(s) in partnership with the Safety Physician.

In Short

• Coordinate and document signal management activities with the product Safety Physician.
• Prepare aggregate safety reports, including project management and quality checks.
• Support RMP updates and REMS reports.
• Perform literature surveillance for marketed and investigational products.
• Prepare materials for Safety Committee meetings.
• Coordinate responses for ad hoc safety queries.
• Support review and analysis of safety content for clinical documents.
• Stay compliant with global PV regulations and guidelines.
• Contribute to process improvement and maintain inspection readiness.
• Perform other tasks as assigned.

Requirements

• 2-3 years relevant medical or pharmaceutical experience.
• Advanced degree (PharmD, RN, MD, PhD, etc.).
• Experience in analysis and interpretation of medical data.
• Excellent oral and written communication skills.
• Ability to work effectively in a team and independently.
• Knowledge of pharmacovigilance and drug development.
• Familiarity with case processing and safety database concepts.
• Proficiency with Microsoft Office Suite and Argus Safety systems.

Benefits

• Competitive salary and annual bonus.
• Comprehensive benefits package including medical, dental, and vision insurance.
• 401(k) retirement plan with company match.
• Generous parental leave and family planning benefits.
• Opportunities for personal and professional growth.