Key Responsibilities:
* Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems
* Collaborate with clinical team on preparation, handling, distribution, filing, and archiving of clinical documentation and reports
* Act as central contact for clinical team for designated project communications, correspondence, and associated documentation
* Mentor less experienced Clinical Trial Assistants (CTAs)
* Participate in departmental quality or process improvement initiatives