Senior Associate Director, Compliance Management

📋 Description

• Lead the generation of timely, actionable quality and compliance insights that inform strategy
• Provide expert GxP compliance guidance to business teams and act as a trusted cross-functional
• Develop and deliver training on Non-Compliance (NC), Corrective and Preventive Action (CAPA), root
• Promote the sharing of quality and compliance best practices across Quality Management and Medicine
• Initiate and support updates to relevant processes, procedures, guidelines, and compliance
• Support global quality issues, compliance topics, and improvement initiatives by helping teams

🎯 Requirements

• Bachelor's and/or Master's degree, such as an MBA, MSc, or a related discipline
• At least 12 years of professional experience within the pharmaceutical or Contract Research
• At least 7 years of experience in Clinical Operations and/or Medicine-related business functions
• Minimum of 5 years of experience managing Non-Compliance (NC) and Corrective and Preventive Action
• At least 8 years of experience working within a Good Practice (GxP) quality management system
• Demonstrated experience interacting with Regulatory Authorities, including supporting or

🎁 Benefits

• Base salary typically ranging from $170,000 to $269,000
• Potential eligibility for a role-specific variable or performance-based bonus and/or additional
• Senior-level exposure to global quality strategy, GxP compliance, clinical development, regulatory
• Opportunities to collaborate with cross-functional and international teams on strategic quality
• Professional growth through involvement in quality transformation, process optimization, risk
• Exposure to clinical operations, regulatory authorities, due diligence, partnering assessments, and