Clinical Supply Chain Manager

About the role

As a Clinical Supply Chain Manager at IQVIA in Reading, you will shape and drive the end-to-end supply strategy for new clinical trials. You will turn complex study protocols into practical kit designs and robust supply plans, working with internal teams and external partners to deliver a supply chain that meets quality standards and study timelines.

Key responsibilities

• Interpret clinical trial protocols to create and run an effective clinical trial supply chain solution.
• Create master English label text in line with the relevant regulatory framework (e.g. Annex 13).
• Create and maintain demand forecasts and packaging plans so packed clinical supplies are ready when needed.
• Initiate packaging campaigns with the assigned vendor and oversee on-time delivery.
• Set up, monitor and update study-assigned Interactive Response Technology (IRT) systems to manage study inventory.
• Create a distribution plan and oversee the assigned vendor(s) carrying it out.
• Track budgets against client-approved quotations and keep projects efficient.
• Manage temperature excursion plans and the review of reported excursions.
• Carry out regular risk management assessments and ensure appropriate mitigations.
• Lead client and vendor meetings on clinical supply chain topics and stay compliant with GxP and regulatory requirements.

Required profile

• Bachelor's degree in a science or business function (preferred but not essential).
• 3-5 years of industry experience in clinical trials (essential).
• 3-5 years of experience in clinical supply chain management (essential).
• Good project management skills and strong communication and direction abilities.
• Strong problem-solving skills and ability to build working relationships with internal and external stakeholders.
• Proficiency in English; the role is not eligible for UK visa sponsorship.

Required skills

• Strong Microsoft Office skills (Word, Excel, PowerPoint).
• GxP knowledge and awareness of regulatory requirements.