At Xogene, we’re revolutionizing the future of clinical trial transparency through AI-powered solutions. Join our team of experts who are transforming how leading pharmaceutical and life sciences companies navigate regulatory compliance. If you're driven by solving complex problems in a qualified setting focused on meaningful and rewarding work, we want to hear from you.
POSITION OVERVIEW
RESPONSIBILITIES
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
personal information.
Authors plain language summaries.
Tracks status and communicates with the client-side Disclosure Coordinators, if needed.
Proactively manages deliverable timelines and ensures project coordinator and management are informed when requirements cannot be met or deliverables are at risk.
Supports all administrative aspects of maintaining US and international clinical trial registry and results database website postings.
Provides continuous process improvement and allow regular constructive feedback to project team members.
REQUIREMENTS
Master's degree students who will complete their post-graduation in 2027
Strong interest in life sciences
Excellent organizational and time management skills and self-starter
Meticulous attention to detail
Robust proficiency with Microsoft Office (Excel, Powerpoint, Word, etc)
Excellent communication skills
Strong sense of teamwork
Intercultural understanding with a global perspective
Knowledge of drug development or clinical science
Bachelor’s degree or 2 years of commensurate experience