Interviewing and consenting subjects for participation.
Arranging collection of blood samples.
Data collection, data entry and data analysis.
preparing summaries of data and related literature related to the current research.
Assist in the generation of reports, posters, abstracts, and articles related to the research project.
Accountable for all tasks in basic clinical studies.
Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
Performs other related work as needed.
Requirements
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Minimum requirements include knowledge and skills developed through
Certifications:
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Bachelor's degree.
Knowledge of medical terminology/environment.
Preferred Competencies
Ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
Ability to communicate with tact and diplomacy.
Strong organizational skills.
Strong communication skills (verbal and written).
Excellent interpersonal skills.
Strong data management skills and attention to detail.
Knowledge of Microsoft Word, Excel and Adobe Acrobat.
Ability to understand complex documents (e.g., clinical trials).
Ability to handle competing demands with diplomacy and enthusiasm.
Ability to absorb large amounts of information quickly.
Adaptability to changing working situations and work assignments.
Application Documents
Resume (required)
Cover Letter (required)
When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
Job Family
Research
Role Impact
Individual Contributor
Scheduled Weekly Hours
40
Drug Test Required
Yes
Health Screen Required
Motor Vehicle Record Inquiry Required
No
Pay Rate Type
Salary
FLSA Status
Exempt
Pay Range
$50,000.00 - $65,000.00 The included pay rate or range represents the University's good faith estimate of the possible compensation offer for this role at the time of posting.
Benefits Eligible
Yes The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook .
Posting Statement
Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.
Benefits
Health insurance
Additional Information
Department
BSD MED - Center for Personalized Therapeutics - Research
About the Department
The Center for Personalized Therapeutics researches pharmacogenomics on two levels: Discovery and implementation. Research Coordinators work on an ongoing implementation project which provides a system for clinicians to use patients' genetic information when making medication decisions.
Job Summary
The Clinical Research Coordinator I focuses on a personalized medicine clinical research study. Responsibilities include interviewing and consenting subjects for participation, arranging collection of blood samples, data collection, data entry and data analysis. Other tasks include preparing summaries of data and related literature related to the current research, and help in the generation of reports, posters, abstracts, and articles related to the research project. These positions are a wonderful opportunity for those anticipating pursuing a degree in Medicine.
Uchicago · Hyde Park Campus