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The Clinical Research Assistant at RUSH University Medical Center plays a vital role in supporting clinical research studies conducted by Principal Investigators (PIs). This position is essential for the successful execution of various types of clinical research, including grant-funded, industry-sponsored, and investigator-initiated studies. The Clinical Research Assistant will be responsible for a range of activities that include the collection, compilation, and documentation of clinical research data. This role requires a commitment to the mission, vision, and values of Rush University Medical Center, and adherence to all relevant policies and procedures. In this position, the Clinical Research Assistant will assist with the recruitment, screening, and scheduling of potential study participants. They will also be involved in the collection and entry of data into study case report forms and electronic data capture systems, ensuring that all queries are addressed promptly. The role may involve the collection and submission of study-related documents, including study protocols and amendments, to the Institutional Review Board (IRB) in accordance with established policies and procedures. Maintaining accurate documentation is crucial, including signed informed consent and HIPAA Authorization forms, relevant IRB approvals, and source documentation. Additionally, the Clinical Research Assistant may be tasked with collecting, processing, and shipping potentially biohazardous specimens, as well as administering structured tests and questionnaires as per research study protocols. The position may also require the use of study-related technology and equipment to facilitate data collection procedures. Preparing study-related materials for participant visits is another key responsibility, ensuring that all necessary resources are available for successful study execution.