Xogene is a leader in innovative technologies and expert services to meet global clinical trial transparency. We offer a dynamic and meritocratic environment with great benefits and flexibility.
Requirements
- Performing clinical trial posting activities for drug, device, and biologic clinical trials
- Performing clinical and non-clinical document redaction to remove confidential information
- Authoring plain language summaries
- Reviewing documents and content as part of a quality check process
- Managing timelines and communicating with internal team and/or stakeholders to ensure compliance
- Tracking status of all active clinical trials and recording clinical trial disclosure activities and compliance
- Supporting administrative aspects of maintaining US and international clinical trial registry and results database website postings
- Acting as a point of contact for inquiries
Benefits
- Mentorship from industry experts working at the intersection of AI technology and business strategy
- Clear career progression path with increasing responsibility as skills develop
- Exposure to cutting-edge AI technologies including LLMs and conversational systems
- Competitive compensation package including comprehensive benefits
- A results-oriented culture that values innovation, responsibility, and professional excellence