Supply Chain Associate

An Associate or Senior Associate – Clinical Trial Supply Management is required to join a leading global pharmaceutical business based in Cork with Hybrid working. This is an opportunity to join a vibrant multi-cultural and multi-lingual team where you will play your part in making a difference for people the world over by supporting the business as it discovers, develops, and delivers medicines that help people live longer, healthier and more active lives.

The Role

• Collaborate with Product Delivery Supply Senior Directors, Clinical Trial Supply Managers, and Molecule Planners to provide expertise in supply chain methodologies while continually looking for internal and external advancements to grow technical expertise and drive processes improvements for productivity and efficiency gains.
• Ensure adequate and timely supply of Clinical Trial (CT) Material to support CT execution.
• Be an active and engaged member of the global trial development team providing expertise around all aspects of clinical supply.
• Translate protocol or planned protocol requirements into demand forecast
• Maintain GMP/GCP compliance by following procedures applicable to CT execution.

• Bachelor’s degree, preferably in health care or sciences related field
• 3+ years work experience in supply chain management or clinical development gained within the Pharmaceutical industry
• Strong project management abilities (timeline, scope, budget, risk management)
• Strong computer skill (i.e. Word, Excel, PowerPoint, Microsoft Project, other)
• Knowledge of Clinical Trail material requirements including GCP and GMP requirements is highly desirable
• Must speak and write fluent English