CDC II

Job Title: Clinical Data Coordinator - Wavre, Belgium

Due to an expansion with one of ICON's exciting key clients, we are currently looking to grow our EU Data Management team in Wavre, Belgium. Both organisations join together with a strong science and technology focus to deliver best in class solutions to the healthcare industry.

Job description:

• Responsible for supporting the team in reviewing CRF/eCRF data for completeness, accuracy, and consistency via computerized edits and manual data checks
• Perform external data reconciliation and serious Adverse Event reconciliation
• Generate and close/resolve (as appropriate) data queries
• Perform User Acceptance Testing and collaboratively work with CDMS personnel to see issues found through re-testing and resolution

Experience required:

• A minimum of 2 years relevant clinical research industry coupled with experience in a data environment.
• Highly computer literate, including strong Microsoft Office skills (Excel, Word, PowerPoint, Project).
• Excellent communication and interpersonal skills, both verbal and written skills.
• Excellent organizational and planning skills as well as a demonstrated aptitude for project management, and the ability to lead more than one project and prioritize accordingly.