Job Summary
A company is looking for a Trial Disclosure Associate.
Key Responsibilities
- Support clinical trial applications through the Clinical Trial Information System (CTIS) and ensure accurate document categorization
- Track CTIS application details and monitor notifications, due dates, and trends
- Communicate project deliverables and timelines effectively across functional areas
Qualifications
- Bachelor's degree (preferably in a health or biological science field)
- 1-3 years of experience in clinical trial registries, regulatory transparency, or drug development
- Background in clinical research, regulatory, or quality within the pharmaceutical industry
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)
- Available to work early hours to support EU colleagues (as early as 7 AM CST)
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