Trial Disclosure Associate

Job Summary

A company is looking for a Trial Disclosure Associate I.

Key Responsibilities

• Support clinical trial applications via Clinical Trial Information System (CTIS) and ensure accurate document categorization
• Track CTIS application details, monitor notifications, and resolve system conflicts
• Assist in ensuring timely disclosure of accurate and complete information globally while maintaining compliance with SOPs

Required Qualifications

• Bachelor's degree required, preferably in a health or biological science field
• 1-3 years of experience in clinical trial registries, regulatory agency transparency, or drug development
• Comfortable learning new systems
• Attention to detail in reviewing documents for accuracy
• Ability to shift daily priorities and meet deadlines