• Process new trial registrations and amendments within the 10-business-day SLA, including reviewing submissions and notifying submitters of acceptance, rejection, or on-hold status.
• Abstract clinical trial administrative and scientific data following established SOPs.
• Code trials using the NCI Thesaurus terminology for disease/condition, intervention, biomarker, and anatomic site data elements.
• Process and validate accrual submissions, including verifying requestor associations and trial registration status.
• Support person and organization curation to ensure data consistency and quality.
• Review header information, protocol documents, and administrative data elements for each trial.
• Follow Good Clinical Practices (GCP) data-handling procedures and guidelines.
• Respond to user inquiries and assist with issue resolution through the ServiceNow ticketing system.
• Participate in the review of clinical research protocols, reports, and statistical analysis plans.
• Support quality assurance and data integrity activities as directed.
