Clinical Data Coordinator II

Key Responsibilities & Duties:

• Thorough knowledge of the data management process
• Excellent organizational, communication, and data management skills (detail oriented)
• Development of data validation specifications
• Test data creation & UAT
• Study status tracking
• Review of data listings
• Maintaining Clinical Study Documents and archiving as appropriate
• Data validation and cleaning
• Conduct SAE & third party data reconciliations
• Represent Data Management at internal / external meetings as appropriate.
• With minimal guidance, manage project timelines and quality issues
• Mentor project team members
• Perform early and final database QC activities
• Database lock activities

1. A minimum of  4  years clinical data management or other relevant experience
2. Experience of at least one of ICON preferred CDMS (Rave, Inform, Oracle Clinical, OCRDC)
3. Highly computer literate, including strong Microsoft Office skills (Excel, Word, PowerPoint, Project)
4.  Strong client relationship management skills, and the aptitude to develop this further