The University of Chicago's Kovler Diabetes Center is looking to solve the problem of diabetes care and research by delivering state-of-the-art comprehensive care, conducting leading-edge research, and partnering with underserved populations.
Requirements
- Knowledge of Microsoft Word, Excel and Adobe Acrobat.
- Understand complex documents, such as clinical trials.
- Prior experience in diabetes and genetics, prior research experience, prior public health and/or community engagement.
Responsibilities
- Coordinates all aspects of conducting research studies including screening, consenting, enrollment, participant follow-up, completion of relevant documents such as case report forms, and adverse event reports.
- Maintains accurate and complete documentation of signed informed consent, relevant IRB approvals, source documentation, case report forms (CRFs), and study related communication.
- Plans and coordinates participant schedule for study procedures.
- 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 participants about study procedures to be performed.
- Performs assessments at visits and monitors for adverse events.
Other
- Minimum requirements include a college or university degree in related field.
- Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.
- Interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
- Strong organizational skills.
- Strong communication skills, both verbal and written.
