Principal Clinical Data Standards Consultant

What you will be doing As a Senior Clinical Data Standards Consultant at ICON Plc, you will be responsible for :

• Developing tools to aid in the implementation and compliance of CDISC, Sponsor, and ICON standards.
• 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, TermiNlogy, ADaM, define-XML and regulatory submission requirements.
• Managing the development and maintenance of data management processes and tools.
• Keeping abreast of industry trends and regulatory updates related to data standards and ensuring their integration into ICONs practices.

Your profile To excel in this role, you should possess the following qualifications and attributes :

What ICON can offer you :

Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include :

Skills Required

Regulatory, Integration, Problem Solving, Clinical Data Management, Communication