The position works under general supervision for routine tasks and with detailed instructions on new assignments
Knowledge of FDA and EMA Regulations, ICH Guidelines, GCP, and familiarity with standard clinical operating procedures
Must be familiar with Word, PowerPoint, and Excel
Excellent verbal and written communication skills
Must be able to work both independently and as part of a team
Tracks and prepares study-specific information utilizing databases, spreadsheets, and other tools
Reviews and participates in the quality assurance of data or documents
Arranges meeting logistics, agendas, and assists with minutes
Interacts with other departments, as directed, to complete assigned tasks
Serves as back up providing verbal and written communication with study personnel
Assists with development of documents and standard forms
Travel may be required

Clinical Project Associate