University of Chicago·Hyde Park, Vermont
The coordinator will manage all aspects of clinical trials, including screening, enrollment, subject follow-up, and maintaining accurate documentation for compliance and study administration. Responsibilities also involve performing protocol procedures, educating patients, monitoring adverse events, and organizing site visits.
BSD MED - Pulmonary - Wolfe Research Staff
About the Department
The Section of Pulmonary/Critical Care has been a model of exemplary patient care, research and post-doctoral training for more than 20 years. The 30 faculty, clinical associates and research associates along with a staff of more than 72 have devoted themselves to the pursuit of excellence in each of these important activities.
The MICU Research Program, with Dr. Krysta Wolfe is looking for a dedicated research coordinator to aid with the development/maintenance of datasets and data collection for a variety of projects related to the care of patients in the intensive care unit.
The Clinical Research Coordinator I (CRC I) provides support to the faculty of the Section of Pulmonary/Critical Care within the Department of Medicine. The CRC I works with the PI, Co-Investigator(s), department, sponsoring agencies, and/or to support and provide guidance on the administration of the compliance, financial and other related aspects of the clinical study.
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.
Certifications: ---
• Bachelor's degree.
• Knowledge of medical terminology/environment.
When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
Scheduled Weekly Hours: 40
$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
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 http://mybenefits.nfp.com/UChicago/benefits-guide/Benefits Guidebook [http://mybenefits.nfp.com/UChicago/benefits-guide/]. [http://mybenefits.nfp.com/UChicago/benefits-guide/]
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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. [http://uchicago.service-now.com/services?id=services_sc_cat_item_request&sys_id=8ff79243dbe91c1029f52ad94b961946]
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Minimum requirements include a college or university degree in a related field along with less than two years of work experience in a related discipline. Preferred qualifications include a Bachelor's degree and knowledge of medical terminology within a clinical environment.
Market context
Clinical Research Coordinator I roles in Vermont are often competitive because employers look for candidates who can support study operations, documentation, and participant coordination while working in a regulated clinical setting. This posting is aimed at early-career applicants with a related degree and limited experience, and it also notes preferred knowledge of medical terminology. Job requirements and benefits here are AI-summarized from the original job description, helping you review fit faster; a practical next step is to compare your coursework or clinical exposure against the listed responsibilities before applying.
