Clinical Research Coordinator
Hyde Park Campus
20126 Anesthesia & Critical Care
About the Unit
The Department of Anesthesia & Critical Care is a clinical academic department at the University of Chicago. The department has been continuously productive not only in its scientific contributions, but also in providing outstanding basic medical care in anesthesiology. Its members have helped to establish the role of anesthesiologists as consultants in fields such as intensive care, oxygen therapy, the recovery room, and inhalation therapy. From a one-member section in 1928, the department has grown to a 60+ member faculty; the department includes 50+ residents, 20+ nurse-anesthetists, 14 administrators and 70+ staff members. Faculty members are active nationally and internationally in the field, and former trainees of the department hold prominent academic positions in the United States and throughout the world.
Works under the general direction of a Clinical Research Manager and the Director of Clinical Research. Works closely with Principal Investigators (PI) and sponsoring agents. Interacts with regulatory agents, Institutional Review Board (IRB) personnel, patients, department staff, and hospital staff. Manages 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.
- Knowledge of patient evaluation and triage procedures and the ability to monitor clinical research patients from many disciplines.
- Thorough working knowledge of medical terminology.
- Knowledge of Microsoft Word and Excel.
- Ability to travel to occasional national and international meetings.
- Demonstrated excellent written and verbal skills.
- Strong organizational and problem-solving skills.
- Demonstrated excellent interpersonal skills.
- Demonstrated ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
- Adaptability to changing working situations and work assignments.
Education and Experience:
- Bachelor's degree or a combination of four years of education and related work experience required.
- Some relevant post-secondary work experience preferred.
- Resume required
NOTE: When applying, all required documents MUST be uploaded under the Resume/CV section of the application
Depends on Qualifications
Scheduled Weekly Hours
Job is Exempt?
Drug Test Required?
Does this position require incumbent to operate a vehicle on the job?
Health Screen Required?
Remove from Posting On or Before
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