Associate Director, Supply Chain

Job summary

The Associate Director, Team Lead for Global Clinical Drug Supply is responsible for overseeing the strategic and operational aspects of drug supply planning for clinical trials. This role involves developing and executing forecasting and supply strategies while ensuring compliance with regulatory standards. The position requires strong leadership to foster a high-performing team and drive cross-functional alignment.

Qualifications

• Bachelor’s degree or equivalent in life sciences, supply chain, procurement, pharmaceutical sciences, engineering, business, or a related field.
• 12+ years of experience in a regulated biotech, pharma clinical supply, or similar environment.
• Proven leadership experience with the ability to coach and motivate team members.
• Extensive knowledge of GMP, GDP, GCP, and documentation standards in a regulated setting.
• Strong communication skills in English, both oral and written.

Responsibilities

• Lead the development and execution of drug supply planning standards and methodologies.
• Drive strategic planning and continuous improvement initiatives within the Global Clinical Drug Supply organization.
• Ensure cross-functional integration across planning, manufacturing, and systems to support supply execution.
• Act as a senior partner to internal and external stakeholders in drug supply planning.
• Oversee project management for clinical programs, ensuring alignment and consistency across trials.

Skills

• Strong prioritization and decision-making abilities in fast-paced environments.
• Ability to balance team leadership with hands-on contributions as a subject matter expert.
• Curiosity and confidence in challenging assumptions and escalating risks.

Education

• Bachelor’s degree or equivalent in a relevant field.

Tools

• Familiarity with supply chain management tools and methodologies relevant to clinical trials.