Senior Set-Up Coordinator

IQVIA · West Lothian, UK

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Role summary

IQVIA Laboratories seeks a Senior Set-Up Coordinator to manage protocol amendments and laboratory database configuration for clinical trials. The role involves designing study implementations using Clinical Trial Management Systems, applying automation and analytics to enhance efficiency, and collaborating with sponsors across the drug development lifecycle. Candidates should hold a life sciences degree with relevant clinical or healthcare experience and demonstrated interest in digital transformation technologies.

What they're looking for

Bachelor's degree in life sciences or related field
1+ years relevant experience in clinical, medical, or healthcare industry
Demonstrated interest or experience with AI, automation, data analytics, or digital transformation
Strong working knowledge of Clinical Trial Management Systems and laboratory data systems
Ability to adapt quickly to new technologies in fast-paced environments
Proactive mindset with curiosity about emerging technologies and innovative solutions

What you'll be doing

Manage end-to-end design and implementation of protocol amendments and sponsor-driven changes
Identify and apply AI-enabled tools, automation, and data analytics to improve study efficiency
Lead design, configuration, and validation of laboratory databases using advanced CTMS platforms
Communicate with sponsors and CROs on technology-enabled study design and delivery
Own amendment delivery, sponsor deliverables, and database quality across study lifecycle

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Date posted24 days ago

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