Onsite Associate Director, Global Clinical Supply
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Supply Chain/Logistics
Supply Chain & Logistics, Regulatory Compliance Specialist, Procurement / Purchasing -
Management
Supply Chain & Logistics, Regulatory Compliance Specialist
Job Description & How to Apply Below
Summit Therapeutics Inc. seeks an Associate Director, Clinical Supply Management to lead global supply chain activities for multiple NSCLC studies.
Based in Princeton, NJ or Palo Alto, CA onsite, you will oversee demand and supply planning, inventory, packaging and labeling, distribution, and regulatory compliance, partnering with CDMOs and IXRS providers. You will manage and develop a CSM team, drive budgets and schedules, and push continuous improvement and risk management across locations to
We would love to welcome a new Onsite Associate Director, Global Clinical Supply to our group in Princeton, NJ, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Onsite Associate Director, Global Clinical Supply role in the description above.
We appreciate your interest in this position.
Join Summit Therapeutics and contribute to our ongoing work.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).