Overview Description: Collaborates with departmental faculty, fellows, and residents on various projects, including but not limited to clinical trial start-up/compliance/ regulatory work, consenting of study subjects, IRB applications, search for grant funding opportunities, database management, library/online searches, statistical analysis, manuscript preparation/editing, educational exhibits, and other academic duties as assigned. Responsibilities Job Requirement: Gather, compile, organize research data. Trace, retrieve electronic medical record charts. Collects data from patient charts, medical records, interviews, questionnaire, and other sources. Responsible for consenting eligible patients for study participation, with local some travel required. Enters collected data into data entry system and ensures accuracy of entered information. Maintains contact with study patients including communication regarding study requirements and other procedures, etc. Understand regulatory process and IRB and FDA requirements, ensuring compliance with regulatory agencies. Attends pertinent educational or study activities and reviews current literature relevant to clinical area. Assists with data gathering for clinical quality reporting requirements. Qualifications Qualification: Education requirements: Medical school graduate (MD, DO - equivalent) Additional details: 12-month PRN rotating contract starting 7/1/2025. Additional duties: Additional duties as assigned. UFPI is an Equal Opportunity Employer and Drugfree Workplace