Senior Clinical Data Coordinator- North Wales, PA

The selected candidate will be responsible for setting up dummy data for testing, generating status reports for management, assisting the DBA with database development, and function as a lead on a study. Responsible for the coordination of project activities and resources, project documentation and interaction with the client company.

Degree in the life sciences or equivalent clinical data work experience. Accuracy/attention to detail is essential. At least 2 years of experience in either a CRO or pharmaceutical company required. Excellent oral and written communication skills are necessary.

ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.