Global PV Scientist - Remote

Overview

The Global PV Scientist is responsible for contributing to the planning, preparation, writing, and review of aggregate reports, and working with affiliates on deliverables related to pharmacovigilance and safety assessment.

In Short

• Contributes to writing and reviewing non-medical portions of aggregate reports.
• Works with internal partners on deliverables.
• Reviews adverse events from clinical trials.
• Participates in the development of safety-related data collection forms.
• Conducts signal detection and evaluation.
• Prepares safety assessment reports.
• Assists in developing risk management strategies.
• Maintains inspection readiness.
• Participates in the implementation of new pharmacovigilance processes.
• Supports regulatory activities for new drug applications.

Requirements

• Master’s or Bachelor's degree.
• Minimum 9+ years of experience in relevant fields.
• Strong background in pharmacovigilance.
• Experience with data analysis and signal detection.
• Familiarity with regulatory requirements and risk management.
• Ability to work collaboratively with cross-functional teams.
• Excellent communication skills.
• Detail-oriented with strong organizational skills.
• Ability to maintain inspection readiness.
• Experience in clinical trial processes.

Benefits

• Opportunity to work with a leading biotechnology company.
• Contribute to innovative human therapeutics.
• Collaborative work environment.
• Professional development opportunities.
• Competitive salary and benefits package.
• Work in a dynamic and impactful field.
• Access to advanced tools and methodologies.
• Engagement in meaningful work that improves health outcomes.
• Flexible working arrangements.
• Supportive team culture.