Freelance QPPV

Overview

Role involves acting as QPPV ensuring compliance with pharmacovigilance legislation.

Ideal candidate has 7+ years of experience in pharmacovigilance and strong knowledge of relevant legislation.

Various EU locations considered

Locations

• Netherlands
• Ireland

Requirements

• Experience as QPPV
• 7+ years in PV systems
• Life Science Degree required
• Fluent in English
• Knowledge of PV legislation
• Experience in audits and inspections
• Knowledge of MS Office

Responsibilities

• Act as QPPV for EU and UK
• Oversee pharmacovigilance activities
• Ensure timely submission of safety reports
• Maintain pharmacovigilance system
• Work with cross-functional teams
• Provide guidance for clinical trials
• Support audits and inspections
• Stay updated on legislation