Principal Clinical Data Standards Consultant

ICON plc · Data

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Full TimePosted Aug 27, 2026

Source: Jobicy

AT A GLANCE
Eligibility
Not available
Category
Data
Salary
Not disclosed
Employment
Full Time
Experience
Senior
Posted
Aug 27, 2026

This role’s source listing does not include Hungary as an eligible location.

ICON plc is seeking a Principal Clinical Data Standards Consultant based in the UK to lead clinical data standards development and compliance. This fully remote role focuses on implementing CDISC standards and providing expert-level guidance for clinical research projects.

As a Principal Clinical Data Standards Consultant, you will act as a subject matter expert to define data collection strategies and maintain internal standards libraries in compliance with regulatory requirements. You will work cross-functionally to drive best practices in clinical data management and mentor junior team members, ensuring high-quality delivery across global clinical trials.

Why You’ll Love This Role

Remote from UK
Full-time contract
Senior level position
Focus on clinical data standards and CDISC compliance
Expert-level subject matter expert role

What You’ll Bring

Bachelor’s degree in Life Sciences, Computer Science, or similar
8+ Years of experience in clinical data management with expertise in data standards
Advanced proficiency in CDISC standards
Knowledge of regulatory requirements such as FDA and EMA
Proficiency in EDC build/design tools including Medidata Rave or Veeva Vault CDMS
Strong leadership capabilities including initiative management and mentorship

What You’ll Get

Benefits not specified in the listing

About the Company

ICON plc is a world-leading healthcare intelligence and clinical research organization. The company focuses on clinical development and drives innovation in healthcare by providing expert services to its global clients.

Listing checked for remote eligibility · Posted Aug 27, 2026 · JobicyApply
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