CTT Specialist - I (Post Graduates - 2027 passouts)

About the role

Xogene combines regulatory expertise with advanced technology to automate complex processes in clinical trial disclosure. As trusted experts with comprehensive knowledge of global regulatory frameworks, we deliver efficient data transformation and regulatory compliance for our clients, streamlining workflows through our AI and agentic networking capabilities.

What you'll do

• Supports the CTT team with data entry components for assigned studies
• Communicates regularly with the CTT team to ensure timelines and deadlines are met
• Enters data directly into the relevant registry systems
• Reviews documents and content as part of a quality check process (an eye for detail is critical, as the data review and entry can be tedious and complex)
• Supports clinical trial document redaction projects to remove or anonymize confidential and

What you need

• 2–5 yrs of experience
• PowerPoint
• Excel
• Process improvement
• Clinical research
• Any graduate