Associate Director, GPV Compliance

Job Summary

To support the development and improvement of GPV compliance systems, the full-time Associate Director, GPV Compliance will manage compliance processes, oversee vendor activities, and ensure alignment with regulatory requirements while working remotely.

Key Responsibilities

• Lead assigned CBM functional areas and contribute to the development of compliance strategies in collaboration with stakeholders
• Coordinate with internal partners and affiliates to ensure compliant practices and effective alliance management
• Oversee vendor activities and manage day-to-day GPV alliance activities, including the facilitation of Pharmacovigilance Committee meetings

Required Qualifications

• Bachelor's degree required
• Minimum 4 years of PV Compliance or Quality Management experience in the pharmaceutical industry
• Experience managing vendor relationships and oversight
• Knowledge of ICH, US, and EU regulations and requirements for pharmacovigilance
• Solid background in pharmaceutical quality system management (GxP)