Trial Disclosure Associate

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)