Teams at University of Southern California

Extracts clinical trial data from medical records into eCRFs/CRFs, maintains regulatory knowledge (SAE reporting), coordinates with sponsors and QA, prepares audit materials, performs patient follow-up and spreadsheet tracking for sponsor invoicing, and ensures data confidentiality and accuracy.

Co-manage campus internship programs, recruit students and employer partners, advise students individually on careers and job-search strategies, support international student advising and experiential education programs, coordinate alumni and employer events, and supervise a student employee.

Coordinate longitudinal observational studies on aging and memory: recruit and enroll participants, schedule and conduct assessments, collect data and biospecimens, maintain regulatory and study documentation, assist with data entry and preliminary analyses, and serve as contact for subjects, IRB, and study personnel.