Principal Clinical Data Standards Consultant

About the role

As a Principal Clinical Data Standards Consultant at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What you'll do

• Your focus will be on coordinating consulting and advisory services delivery, resolving issues, and developing team capability
• Collaborating with cross-functional teams to define data collection strategies and standards for clinical trials
• Developing and maintaining training and reference materials related to standards topics including CDASH, SDTM, Terminology, ADaM
• Managing the development and maintenance of data management processes and tools

What you need

• 8–14 yrs of experience
• SAS
• Clinical data management
• Learning and development
• R
• Clinical research
• PLC
• B.Sc or B.Tech or B.E. or BCA