University of Chicago
Clinical Research Coordinator
The Clinical Research Coordinator supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study. This position offers you the opportunity to lead patient recruitment, coordinate study visits, and conduct informed consent discussions while ensuring protocol adherence and patient safety. The Clinical Research Coordinator will oversee specimen handling, perform study assessments, manage case report forms and adverse event documentation, and safeguard patient data. In addition, this position will liaise with principal investigators, sponsors, CROs, and regulatory bodies, and prepare and maintain IRB submissions and approvals. Responsibilities include managing all aspects of clinical trials from start-up through close-out, leading patient recruitment, overseeing specimen handling, and liaising with principal investigators and regulatory bodies. The Clinical Research Coordinator will also prepare and maintain IRB submissions and approvals. Minimum qualifications include a college or university degree in a related field and less than 2 years of work experience in a related job discipline. Preferred qualifications include experience in conducting oncology trials and research.
The Clinical Research Coordinator supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study. This position offers you the opportunity to lead patient recruitment, coordinate study visits, and conduct informed consent discussions while ensuring protocol adherence and patient safety. The Clinical Research Coordinator will oversee specimen handling, perform study assessments, manage case report forms and adverse event documentation, and safeguard patient data. In addition, this position will liaise with principal investigators, sponsors, CROs, and regulatory bodies, and prepare and maintain IRB submissions and approvals. Responsibilities include managing all aspects of clinical trials from start-up through close-out, leading patient recruitment, overseeing specimen handling, and liaising with principal investigators and regulatory bodies. The Clinical Research Coordinator will also prepare and maintain IRB submissions and approvals. Minimum qualifications include a college or university degree in a related field and less than 2 years of work experience in a related job discipline. Preferred qualifications include experience in conducting oncology trials and research.