CTT Team Member

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

• Performing clinical trial protocol registration and results posting activities for drug, device, and biologics clinical trials
• Performing clinical and non-clinical document redaction to remove and/or anonymize personal identifiable information (PII) and company confidential information (CCI)
• Authoring plain language summaries of clinical documents including protocol and results of clinical trials for disclosure
• Reviewing documents and content as part of a quality check process
• Managing timelines and communicating with internal team and/or stakeholders to ensure compliance

What you need

• 1–4 yrs of experience
• PowerPoint
• Excel
• Clinical research
• Process improvement
• B.Sc