Strategic Lead, Clinical Trial Supply Chain

IQVIA Holdings Inc.; Reading; On-site; GBP 60,000 - 85,000; Full time

Job summary

IQVIA Holdings Inc. is seeking a Clinical Supply Chain Manager to shape end-to-end supply strategy for new clinical trials. You will translate study protocols into robust supply plans and collaborate with internal teams and external partners to ensure quality and on-time delivery.

The role requires 3-5 years in clinical trials and supply chain, strong project management, and proficiency in English and Microsoft Office. You will oversee budgeting, IRT systems, labeling, and regulatory compliance.

Qualifications

• Bachelor's Degree in a science or business function is preferred.
• 3-5 years of industry experience in clinical trials.
• 3-5 years experience in clinical supply chain management.
• Strong communication and problem-solving skills.

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 (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.
• Lead client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates.
• Create a Temperature Excursion management plan.
• Manage the review and assessment process of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team.
• Conducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed.

Skills

Project management

Stakeholder management

Communication

Microsoft Office

English language

Education

Bachelor's degree in science or business

Tools

IRT systems

Job description

IQVIA Holdings Inc. is seeking a Clinical Supply Chain Manager to shape end-to-end supply strategy for new clinical trials. You will translate study protocols into robust supply plans and collaborate with internal teams and external partners to ensure quality and on-time delivery.

The role requires 3-5 years in clinical trials and supply chain, strong project management, and proficiency in English and Microsoft Office. You will oversee budgeting, IRT systems, labeling, and regulatory compliance.