Global Clinical Trial Operations Intern
Core
Support local clinical trial operations including site administration, document management, meeting planning, and site readiness coordination under the oversight of CRA/CRA-Manager.
Role type
Clinical Trial Operations Intern
Builds
Clinical trial site readiness and operational support for local studies
Domain
Clinical Research / Pharmaceutical Trials
Deliverable
client delivery
Required skills
Document Management, Database Management, Meeting Management, Site Management, Regulatory Documentation, Data Entry, IT Automation, Video Editing, Coding, AI
Preferred skills
None stated
Technologies
CTMS, eTMF, Automation tools, Coding frameworks, AI tools
Responsibilities
Track and report essential documents and safety reports; Prepare and archive clinical documents including Investigator trial files; Organize local investigator meetings and support vendor coordination; Coordinate site readiness tasks and assist with site visits (initiation, monitoring, close-out); Manage regulatory documentation for study start-up and close-out.
Seniority
Intern/Co-op
