Associate Director, Global Clinical Drug Supply (Pharmaceutical, Copenhagen)

Job summary

This role involves leading a team within Global Clinical Drug Supply Manufacturing, focusing on sourcing and supplying clinical trial materials for late-stage trials. The position emphasizes high-quality supply management and operational excellence in a regulated environment.

Qualifications

• Bachelor’s degree or equivalent in life sciences, supply chain, procurement, or related fields.
• Significant experience in biotech, pharma, or clinical supply environments.
• Proven leadership experience with the ability to coach and develop team members.

Responsibilities

• Lead and develop a high-performing team, ensuring engagement and accountability.
• Set operational standards and priorities, fostering a compliant culture.
• Drive sourcing and supply activities to ensure reliable clinical trial support.
• Establish vendor governance practices in collaboration with various stakeholders.
• Monitor market dynamics and translate insights into actionable strategies.
• Build relationships with vendors and internal stakeholders for timely supply delivery.
• Oversee supplier performance and manage risks affecting timelines and compliance.
• Partner with cross-functional teams to support effective execution of clinical supply.
• Contribute to the development of sourcing-related SOPs and continuous improvement initiatives.

Skills

• Strong leadership and team management skills.
• Expertise in sourcing, vendor management, and clinical drug supply activities.
• Solid understanding of GMP, GDP, and GCP standards.
• Ability to drive cross-functional projects in a global setting.

Education

• Bachelor’s degree or equivalent in relevant fields.

Tools

• Familiarity with vendor management systems and compliance documentation standards.