About the Role

This position involves supporting the Clinical Trial Information System (CTIS) application processes, ensuring the accurate and timely disclosure of clinical trial information globally. The role requires effective communication across departments and adherence to current standard operating procedures.

Responsibilities

• Support CTIS application processes, including document upload and quality control. 
• Track and monitor CTIS application metrics, notifications, due dates, and trends.
• Identify and resolve system conflicts or escalate as necessary.
• Ensure timely and accurate global disclosure of clinical trial information.
• Communicate deliverables, timelines, and process updates across departments.
• Stay compliant with current SOPs and work instructions; participate in cross-training.

Education Qualification

• Bachelor’s degree, preferably in health or biological sciences.

Required Skills 

• 1–3 years of experience in clinical trial registries, regulatory transparency, or drug development, preferably within the pharmaceutical industry.
• Strong attention to detail and ability to identify and correct inconsistencies or errors.
• Comfortable learning and navigating new systems.
• Strong time management skills with the ability to shift priorities and meet deadlines.
• Proficiency in MS Office Suite.
• Ability to work effectively in a global team and start as early as 7 AM CST to support EU colleagues.