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You will be updated with latest job alerts via emailInterpret clinical trial protocols to create and execute an effective clinical trial supply chain solution
Create master English label text in accordance with relevant regulatory framework (e.g. Annex 13)
Create and maintain demand forecasts and packaging plans so that packed clinical supplies are readily available in
accordance with the project requirements
Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery
Setup monitor and where necessary update study assigned Interactive Response Technology (IRT) systems to ensure
study inventory is effectively managed
Create an appropriate distribution plan and have oversight of the assigned vendor(s) executing it
Ability to work independently and proactively to ensure that the supply of all trial materials is delivered to the right place at the
right time
Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved
quotations
Maintains 100% compliance on all assigned training and applies learnings to everyday practice
Remain up to date in all GxP and regulatory requirements applicable to the role
Leads client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates
Creates a Temperature Excursion management plan
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
Manager
Full-Time