WHY XOGENE?At Xogene, we believe work should be enjoyable, meaningful and promote work-life balance. Working with us means joining a vibrant community of like-minded individuals who are passionate about what they do. If you thrive in a fast-paced, innovative environment and want to be part of a global team that is shaping the future of clinical trial transparency services bolstered by our suite of modern and AI-powered technology products, we would love to hear from you. Make a difference and build a rewarding career with Xogene.
POSITION OVERVIEW
Offering a suite of services and software products, Xogene is a leader in innovative technologies and expert services to meet global clinical trial transparency. Combining deep transparency expertise with a modern technology stack, Xogene provides software solutions. We develop innovative, configurable solutions that include the first end-to-end transparency platforms to meet disclosure requirements and custom sponsor trial websites for patient engagement.
As we continue to expand, we are seeking an experienced Clinical Trials Transparency Junior Analysts to join our dynamic team and contribute to our ongoing growth and success. The Clinical Trials Transparency Junior Analyst (“Jr. Analyst”) supports aspects of the clinical trial transparency offerings including entering clinical study data from source documents directly into the clinical trial registry system (i.e. Clinicaltrials.gov, EudraCT, etc.), redacting documents. At times, the CTTJA will be required to perform quality checks (QC) within the group, so attention to detail is a must. The Xogene Junior Analyst is an integral member of the organization, performing a diverse range of operational activities that directly impact the success of the clinical trial transparency projects. This role requires attention to detail, a positive and strong teamwork, excellent writing skills and experience interacting in multi-cultural, global working environment.
KEY TASKS AND RESPONSIBILITIES.
•Supports the CTT team with data redactions for assigned documents
• Communicates regularly with the CTT team to ensure timelines and deadlines are met
• Conduct peer review of documents and content from the anonymization tool 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
• Proactively manages deliverable timelines and ensures project coordinator and management are informed when requirements cannot be met or deliverables are at risk
REQUIREMENTS
• Bachelor’s degree in science (Pursuing Bachelors and would graduate by 2025)
• Strong interest in life sciences
• Excellent organizational and time management skills and self-starter
• Meticulous attention to detail
• Strong 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