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Clinical Trial Assistant - Clinical Supplies
ICON Clinical Research
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Reading, United Kingdom
Location
Reading
Posted
June 22, 2026
Commute
Local Area
Local Opportunity Near You!
This job is in your area. Enjoy a short commute and work close to home.
Job Description
Harlow, Essex based - 2 days a week in theoffice requirement
ICON plc is a world-leading healthcare intelligence and clinical research organization. Weβre proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Senior Clinical Supply Specialist at ICON, you will oversee the management and distribution of clinical trial supplies, ensuring that all materials are delivered efficiently and in compliance with regulatory requirements.
2 Days a week based in the office in Harlow, Essex
**What You Will Do:**
You will take ownership of clinical supplies and logistics deliverables, applying your expertise to complex challenges.
Key responsibilities include:
+ Work within a global team. Create master label content according toexisting processes and procedures, designing Clinical Trial labels.
+ Perform quality critica...
ICON plc is a world-leading healthcare intelligence and clinical research organization. Weβre proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Senior Clinical Supply Specialist at ICON, you will oversee the management and distribution of clinical trial supplies, ensuring that all materials are delivered efficiently and in compliance with regulatory requirements.
2 Days a week based in the office in Harlow, Essex
**What You Will Do:**
You will take ownership of clinical supplies and logistics deliverables, applying your expertise to complex challenges.
Key responsibilities include:
+ Work within a global team. Create master label content according toexisting processes and procedures, designing Clinical Trial labels.
+ Perform quality critica...