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
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