Clinical Operations Intern
July 2013 — Present
• Utilize the Clinical Trial Management System (CTMS) to ensure investigator recruitment activities are accurately tracked.
• Perform essential document collection, review, maintenance, and close-out activities.
• Perform study tracking via CTMS or Sponsor designated system to ensure that the study files are current, accurate, and complete.
• Liaise with project team members regarding study site issues.
• Provide administrative assistance to clinical team members (IHCRAs, CRAs, CTMs) as needed such as creating site binders and shipping materials.
• Contribute to the Spanish Translation QC team on an as needed basis.