Regulatory Affairs Lead Director - Remote

Overview

The Lead Director, Regulatory Affairs will play a crucial role in supporting McKesson’s Controlled Substances Monitoring Program, ensuring compliance and operational excellence in the pharmaceutical sector.

In Short

• Lead customer due diligence reviews for compliance with CSMP policies.
• Oversee due diligence completion by CSMP personnel.
• Act as a training contact for new hires and existing team members.
• Review CSMP reports and analytics to guide customer due diligence.
• Identify trends and refine policies within the CSMP.
• Drive performance and productivity of team members.
• Maintain confidentiality and stakeholder trust.
• Evaluate complex scenarios for informed decision-making.
• Demonstrate strong analytical and organizational skills.
• Possess specific knowledge of the Controlled Substances Act.

Requirements

• 10+ years of experience in controlled substance compliance.
• Undergraduate degree or equivalent experience required.
• Ability to manage multiple initiatives in a dynamic environment.
• Excellent written and verbal communication skills.
• Strong attention to detail and commitment to accuracy.
• Proven problem-solving mindset.
• Must be authorized to work in the US without sponsorship.
• Ability to travel up to 15%.

Benefits

• Competitive compensation package including base pay and bonuses.
• Comprehensive benefits for health and well-being.
• Opportunities for growth and impact within the organization.
• Diverse and inclusive work environment.