Clinical Supply Chain Manager

Role & responsibilities

• Interpret 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

• 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