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 :

Skills Required

Collaboration, cross functional team , Clinical Data Management