Clinical Supply Chain Manager

IQVIA

. Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution .

Posted 9/29/2026full-timeReading • United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Trial Supply Chain Management and project management, ensuring compliance with GxP and regulatory requirements while effectively collaborating with stakeholders. Proficient in creating demand forecasts, managing budgets, and executing clinical trial protocols.

Highest-signal resume keywords

Clinical Trial Supply Chain ManagementProject Management SkillsGxP ComplianceDemand ForecastingEffective Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Protocol InterpretationTemperature Excursion ManagementInteractive Response Technology (IRT) SystemsBudget TrackingMaster English Label Text Creation

Soft Skills

Problem SolvingRelationship BuildingEffective Communication

Tools & Technologies

Microsoft Office Suite

Industry Keywords

Clinical TrialsRegulatory FrameworksAnnex 13Risk ManagementVendor Management

About the role

Key responsibilities & impact

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 frameworks, such as Annex 13
Create and maintain demand forecasts and packaging plans
Initiate packaging campaigns with assigned vendors and oversee on-time delivery
Set up, monitor, and update study-assigned Interactive Response Technology (IRT) systems
Create distribution plans and oversee assigned vendors executing them
Ensure trial materials are delivered to the right place at the right time
Track budgets to ensure efficient project execution within client-approved quotations
Maintain 100% compliance with assigned training and apply learnings in daily practice
Remain current on applicable GxP and regulatory requirements
Lead client and vendor meetings concerning clinical supply chain topics or status updates
Create a Temperature Excursion management plan
Manage review and assessment of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team
Conduct regular risk management assessments and execute appropriate mitigations

Requirements

What you’ll need

Bachelor's Degree in a science or business function (Preferred not essential)
3-5 years industry experience in Clinical Trials (Essential)
3-5 years experience in Clinical Supply Chain Management (Essential)
Ability to demonstrate good project management skills
Ability to create effective working relationships with internal and external stakeholders
Ability to demonstrate effective communication and direction
Ability to problem solve
Strong Microsoft Office skills (Word, Excel, PowerPoint, etc.)
Proficient in the English language
Not eligible for UK visa sponsorship