University of Chicago
Clinical Research Coordinator I
University of Chicago, Chicago, Illinois, United States, 60290
Clinical Research Coordinator I
The Clinical Research Coordinator I provides support to the faculty of the Section of Hematology/Oncology within the Biological Sciences Division. The CRC1 will be involved in multiple research trials types, multi-centered cooperative group and intergroup studies, at a national level, multi-institutional pharmaceutical trials, and multi-centered trials designed, implemented and coordinated in the Section. Responsibilities include: Coordinates all aspects of conducting clinical trials including screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports. Maintains accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication. Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules. Ensures standard operating procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications. Prepares and maintains protocol submissions and revisions. Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and potential side effects. Performs assessments at visits and monitors for adverse events. Organizes and attends site visits from sponsors and other relevant study meetings. May recruit and interview potential study patients. May obtain, possess, and transport specimens to appropriate laboratory according to established aseptic techniques. Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups. Accountable for all tasks in basic clinical studies. Assists with various professional, organizational, and operational tasks under direct supervision. Performs other related work as needed. 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 a bachelor's degree, proficiency in Microsoft Word, Excel, and Adobe Acrobat, and a range of competencies including strong organizational skills, communication skills, and data management skills. Application documents required include a resume/CV and cover letter. The role is a research individual contributor with scheduled weekly hours of 37.5. Drug test and health screen are required. The pay rate is $50,000.00 - $65,000.00 and the role is benefits eligible.
The Clinical Research Coordinator I provides support to the faculty of the Section of Hematology/Oncology within the Biological Sciences Division. The CRC1 will be involved in multiple research trials types, multi-centered cooperative group and intergroup studies, at a national level, multi-institutional pharmaceutical trials, and multi-centered trials designed, implemented and coordinated in the Section. Responsibilities include: Coordinates all aspects of conducting clinical trials including screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports. Maintains accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication. Plans and coordinates patient schedule for study procedures, return visits, and study treatment schedules. Ensures standard operating procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications. Prepares and maintains protocol submissions and revisions. Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and potential side effects. Performs assessments at visits and monitors for adverse events. Organizes and attends site visits from sponsors and other relevant study meetings. May recruit and interview potential study patients. May obtain, possess, and transport specimens to appropriate laboratory according to established aseptic techniques. Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups. Accountable for all tasks in basic clinical studies. Assists with various professional, organizational, and operational tasks under direct supervision. Performs other related work as needed. 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 a bachelor's degree, proficiency in Microsoft Word, Excel, and Adobe Acrobat, and a range of competencies including strong organizational skills, communication skills, and data management skills. Application documents required include a resume/CV and cover letter. The role is a research individual contributor with scheduled weekly hours of 37.5. Drug test and health screen are required. The pay rate is $50,000.00 - $65,000.00 and the role is benefits eligible.