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Paula O'Reilly
Life Science

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Details

Clinical Trial Supply Management Associate


Reference:POR/ 662861 Location: Cork
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Supply Chain Specialist

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.

The Person

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




For further details please contact; Paula O’Reilly on 00 353 (0)87 7094141 or send CV in confidence to [email protected]