Job Description:

RESPONSIBILITIES

• Enter and extract clinical trial data into data collection tools (Epic, Excel)
• Conduct quality control review of clinical trial data
• Conduct data review of CRFs, eCRFs, reports, or data listings, as applicable
• Generate, track, and close queries for images, reports, CRFs, eCRFs, as applicable
• Conduct data/image transfers, as applicable
• Track conduct of DE/QC activities
• Maintain both paper and electronic project files in accordance with standard operating procedures
• Advocate compliance with all standard operating procedures
• Contribute to generation study specific reports
• Contribute to generation of study specific data collection tools/databases
• Update appropriate study team members and management with task, deliverable, and project statuses.
• Coordinate efforts to ensure on time completion of high quality deliverables to both internal and external partners and customers
• Perform other tasks as needed

Experience:

• Bachelors in Life Sciences
• Research experience
• Epic and Excel experience required