Clinical Supply Chain Manager

Role Overview

• 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
• Provide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations
• 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
• Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed

Requirements

• High School Diploma or equivalent
• 2-3 Years related industry experience in Clinical Trials
• 2-3 Years experience in Clinical Supply Chain Management
• Advanced English level
• Strong Microsoft Office skills (Word, Excel, Powerpoint etc)
• Ability to demonstrate good project management skills
• Ability to create effective working relationships with internal and external stakeholders

Benefits

• Maintains 100% compliance on all assigned training and applies learnings to everyday practice