Clinical Trial Supply Chain Lead

Appcast; Reading; On-site; GBP 65,000 - 90,000; Full time

Job summary

IQVIA is seeking a Clinical Supply Chain Manager to shape end-to-end supply strategy for new clinical trials in Reading, UK. You will translate study protocols into smart kit designs and robust supply plans, collaborating with internal teams and external partners to meet quality standards and study timelines.

You will manage demand forecasts, packaging campaigns, IRT systems, distribution plans, and budget tracking, while ensuring compliance with GxP and regulatory requirements and leading

Qualifications

• Bachelor's degree in science or business.
• 3–5 years of industry experience in Clinical Trials.
• 3–5 years experience in Clinical Supply Chain Management.
• Ability to demonstrate good project management skills.
• Ability to build working relationships with stakeholders.
• Strong communication and leadership abilities.
• Proficient in English.

Responsibilities

• Interpret clinical trial protocols to create and execute a clinical trial supply chain solution.
• Create master English label text in accordance with regulatory framework (e.g. Annex 13).
• Create and maintain demand forecasts and packaging plans for project requirements.
• Initiate packaging campaigns with vendor and oversee on-time delivery.
• Setup and monitor study IRT systems to manage inventory.
• Create distribution plan and oversee vendor execution.
• Ensure delivery of trial materials to the right place, on time.
• Track budgets and stay in line with quotations.
• Maintain 100% training compliance and apply GxP knowledge.
• Lead client and vendor meetings on supply chain topics as needed.
• Develop Temperature Excursion management plan.
• Review Temperature Excursions with IQVIA team.

Skills

Project management

Stakeholder management

Problem solving

MS Office

English proficiency

Education

Bachelor's degree in science or business

Job description

IQVIA is seeking a Clinical Supply Chain Manager to shape end-to-end supply strategy for new clinical trials in Reading, UK. You will translate study protocols into smart kit designs and robust supply plans, collaborating with internal teams and external partners to meet quality standards and study timelines.

You will manage demand forecasts, packaging campaigns, IRT systems, distribution plans, and budget tracking, while ensuring compliance with GxP and regulatory requirements and leading