Research Analyst

• Assists with clinical, regulatory, business, and other documentation associated with oncology research projects/clinical trials within LCI
• Participates in the study project start-up activity, working with the PI and others to initiate new research projects
• Maintains protocol amendments, deviations, and informed consent changes regarding oncology research studies, assuring all documentation is managed compliantly and maintained in an audit-ready manner
• Maintains appropriate documentation for assigned studies
• Assists in maintenance of filing systems, data repositories and systems
• Assists in the monitoring of clinical trial compliance by reporting issues and problems appropriately
• Obtains required documentation to assess patient eligibility for research studies
• Prepares and submits information from patient's chart and other source documents on appropriate data forms/flowsheets/databases
• Assists with inventory, ordering, organization and distribution of supplies related to assigned trials
• Completes registration for patient enrollment and maintains status in sponsor and LCI databases
• Assists with the coordination of research monitor visits and audits

Registered Nurse, Oncology Research Specialist

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