SP - Clinical Research Assistant

Position Summary At UConn Health this position is responsible for independently performing a full range of tasks for assigned clinical research projects/programs or segments of programs/projects. Supervision Works under general supervision of an employee of higher grade when performing advanced tasks; works independently in the performance of routine research duties. Examples of Duties Performs a range of duties in conducting clinical research, provides support services for assigned research projects. Performs tests and interacts with patients. Coordinates the facilitation of clinical research protocols. Prepares IRB applications, consent and annual renewals. May prepare study progress reports and protocol amendments. Coordinates the procurement, preparation and shipping of research specimens. Assists higher-level research staff on assigned projects. Prepares all necessary materials required for audits or monitoring visits. Prepares summaries of research results. Assists in preparation and presentation of research findings, grant and contract applications. Receives training in designated research protocols, procedures and techniques that the supervisor deems appropriate such as phlebotomy, ECG and equipment (centrifugation). Performs related duties as required. Minimum Qualifications Required Knowledge, Skill & Ability Knowledge of research protocols, principles and procedures. Knowledge of aspects of clinical trials such as screening, interviewing, case report forms. Knowledge of experimental design, mathematics, statistics, computer applications and computer data management. Oral and written communication skills. Knowledge of a science such as biology or psychology. Ability to identify, produce, organize, evaluate and interpret data. Knowledge of ethics and regulatory procedures (i.e., informed consent, IRB applications, data safety and monitoring plans) involved with clinical trials and other clinical research. Ability to work as a member of a project team; knowledge of clinical tasks required for research (e.g., phlebotomy, centrifugation, interviewing). Experience and Training General Experience: Bachelor's degree in the appropriate scientific discipline, e.g., Biology or Psychology plus one (1) year of clinical research experience in a relevant discipline. Degrees in other areas may be substituted on a case-by‑case basis. Substitution Allowed: Certification as a Clinical Research Professional (CCRP) by SOCRA or an equivalent with six (6) years of appropriate practical clinical research experience may be substituted for the Bachelor's degree. If not certified at the time of hire, must take and pass the certification within one (1) year of employment. Working Conditions Incumbents in this class may be exposed to communicable/infectious disease. Special Requirements This position may involve local or out‑of‑state travel. Incumbents in this classification may be required to work some evenings and weekend hours. Schedule This position is full‑time, 40 hours per week, Monday through Friday from 8:00 am to 5:00 pm with some evening/weekend hours to meet study requirements. Position Status This is a temporary grant‑funded position with a projected end date of September 25, 2026. Due to the special nature of this position, continuous employment cannot be guaranteed. Employment and Equal Opportunity Policies The University of Connecticut Health Center is an affirmative action employer, in addition to an EEO and M/F/V/PWD/PV employer. All employees are subject to adherence to the State Code of Ethics. #J-18808-Ljbffr Uconn Health Center