Clinical Research Assistant I, Internal Medicine Digestive and Liver

Works under the direction of an Investigator with general supervision to primarily provide ongoing data management for local and national research studies. May coordinate observational (non-treatment) studies. Performs tasks such as entering and maintaining study data, supporting data queries and regulatory submissions, maintaining databases, scheduling research visits, assisting with protocol-related tasks, preparing IRB reports, reviewing medical records for eligibility, recruiting and enrolling participants, maintaining research supplies, collecting specimens, and performing basic study procedures (e.g., phlebotomy, vital signs, EKG) under supervision. May also interact with patients or research participants and maintain or modify records. Performs other duties as assigned. Benefits PPO medical plan, available day one at no cost for full‑time employee‑only coverage Paid Time Off, available day one Retirement Programs through the Teacher Retirement System of Texas (TRS) Paid Parental Leave Benefit Wellness programs Tuition Reimbursement Public Service Loan Forgiveness (PSLF) Qualified Employer Licenses and Certifications BLS (Basic Life Support) may be required based on study protocols or location requirements. CPR AED may be required based on location requirements Job Duties Enters data into case report forms or other data collection systems based on research studies; assists with maintenance of study level documentation. Assists with data queries and possible edits for accuracy. Compiles data for regulatory requirements and/or deadlines for local or sponsor submissions. Maintains existing databases and ensures data integrity. Understands visit schedules, criteria and protocol requirements for routine and low complexity trials (e.g., questionnaire, data registry, scripted); schedules research visits. Assists research staff by completing research protocol related tasks. Assists with preparing annual reports and/or modifications to the institutional review board (IRB), including reportable events (UPIRSO). Reviews and abstracts information from medical records, including eligibility criteria. Recruits and enrolls patients in research studies, including consenting patients after training and with supervision. Assists with ordering and maintaining research supplies following university/department procedures, ensuring equipment is in good working order. With adequate training and supervision, assists with collecting and processing specimens following established procedures/protocols. Assists in preparing studies for closeout, e.g., packing files, documenting files for storage, shipping extra supplies back to sponsor. With adequate training/credentialing and supervision, performs study procedures such as phlebotomy, vital signs, and EKGs needed for research studies. Other procedures may be required depending on the study. Duties may include interacting with or caring for patients or research participants, maintaining or modifying records (patient or research), or handling financial records, as relevant to the study. Performs other duties as assigned. Security and EEO Statement This position is security‑sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information. UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal‑opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status. #J-18808-Ljbffr