Clinical Research Associate

Responsibilities

• •Provide input and assist with harmonization of Clinical Operations databases and tracking tools
• •Assist in the maintaining clinical information and training of Clinical Operations personnel in the clinical trials database
• •Processes re-supply drug shipments
• •Order and maintain inventory of clinical supplies
• •Order and ships case report forms
• •Assists with development of documents for site binders
• •Assembles and coordinates distribution of site binders
• •Serves as CRA back up providing verbal and written communication with study personnel
• •Under close supervision reviews and participates in the quality assurance of data or documents
• •Arranges meeting logistics
• •Rafts meeting agendas and assists in preparing meeting minutes
• •The position interacts with other departments, as directed, to complete assigned tasks
• •May assist with monitoring visits under the direct supervision of senior staff
• •Travel may be required
• •Assist with the planning and facilitation of investigator meeting and, when applicable, provide on location support during the meetings
• •12 more items(s)