GCP Compliance Associate Director

Job Summary

A company is looking for an Associate Director, GCP Compliance.

Key Responsibilities

• Direct and implement compliance management for clinical trial delivery functions, including quality events and internal audits
• Establish and lead proactive risk-based compliance assessments and develop CAPA/EC-related compliance strategies
• Develop and report key performance indicators and mitigation strategies for clinical trial delivery compliance

Required Qualifications, Training, and Education

• Bachelor's Degree or international equivalent required; Life Sciences preferred
• 8+ years of experience in the pharmaceutical industry and/or clinical research organization, including 6+ years in compliance or clinical study management
• Experience in leading projects and coordinating collaboration with cross-functional teams
• Global/international experience required
• Operational experience in clinical development with exposure to novel approaches