Clinical Research Assistant

Clinical Research Coordinator/Assistant Opportunity w/ Large CRO!

Clinical Research Assistant

• Verify and/or correct research study information on source documents
• Research queries and variances, and provide feedback to the site data collector
• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness
• Prepare and maintain research study files
• Compile, collate and submit study information within established deadlines
• Assist in maintenance of regulatory documentation
• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits
• Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget
• Processing of required lab specimens, labeling of vials, and accurately filling out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations
• Perform various administrative support functions such as reception, office organization, and office supply management 

Qualifications

Bachelor’s Degree

Must have a minimum of 1 year of clinical site experience; drug trial experience  

Must have a minimum of 6 months of EDC experience

Schedule

Onsite Monday-Friday Monday through Friday 8:00 AM-5:00 P