Clinical Research Coordinator 1
University of Chicago
Hospital Medicine is a rapidly growing field within internal medicine where physicians, called ‘Hospitalists’, focus their practice on the care of hospitalized patients. Although clinical needs have been the driving force behind the growth of Hospital Medicine nationally, our program has always had a major academic focus on research, quality improvement, and teaching. The Comprehensive Care Physician (CCP) Program is an innovative program within the Section of Hospital Medicine that provides patients with complex medical and social needs a physician who cares for them in both, the hospital and the clinic.
About the Department
The CCP model has been studied in a randomized trial since 2012 with funding from the Center for Medicare and Medicaid Innovation (CMMI) and has shown statistically significant improvements in patient experience and health outcomes and decreases in hospitalization and spending. In addition, this model and study have evolved to since better engage patients and address social determinants of health. Since 2016, first with funding from the Robert Wood Johnson Foundation and now from the Patient-Centered Outcomes Research Institute (PCORI), we have created the Comprehensive Care Community and Culture Program (C4P), which adds to CCP: 1) systematic screening of unmet social needs, 2) access to a community health worker, and 3) access to community-based arts and culture programming. C4P is also being evaluated through a randomized trial and has produced promising preliminary findings, particularly in activating patients.
The Clinical Research Coordinator 1 (CRC1) is an entry level researcher working with the Principal Investigator (PI) Dr. David Meltzer, Co-Investigator(s) and other study personnel, and under the limited direction of departmental, Research Director. The CRC1 works with the PI, Co-Investigator(s), department, sponsoring agencies, and/or the to support and provide guidance on the administration of the compliance, financial and other related aspects of the clinical study.
Coordinates the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.
Organizes and attends site visits from sponsors and other relevant study meetings.
Protects patients and data confidentiality by ensuring security of research data and personal health information and compliance with federal regulations and sponsor protocols.
Ensures Standard Operating Procedures (SOP) are implemented and documented in accordance to study sponsor, primary investigator, and regulatory agency specifications.
Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication.
Understands the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions.
Understands the federal research regulations and identifies the federal research organizations’ role in regulating human research participation.
Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
Performs other related work as needed.
Education:Minimum requirements include vocational training, apprenticeships or the equivalent experience in related field (not typically required to have a four-year degree).
Previous research or relevant experience.
Knowledge of medical terminology/environment.
Technical Skills or Knowledge:
Knowledge of Microsoft Word, Excel and Adobe Acrobat.
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.
Ability to read and 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.
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.
Scheduled Weekly Hours
Drug Test Required
Health Screen Required
Motor Vehicle Record Inquiry Required
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Staff 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.
We seek a diverse pool of applicants who wish to join an academic community that places the highest value on rigorous inquiry and encourages a diversity of perspectives, experiences, groups of individuals, and ideas to inform and stimulate intellectual challenge, engagement, and exchange.
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