This job was posted by https://illinoisjoblink.illinois.gov : For moreinformation, please see:https://illinoisjoblink.illinois.gov/jobs/11598439 Department

　　BSD MED - Endocrinology - Kovler Research Staff

　　About the Department

　　The Clinical Research Coordinator 2 will work as part of the KovlerDiabetes Center in the Department of Medicine, Section of Adult andPediatric Endocrinology, Diabetes, and Metabolism at the University ofChicago. The Section of Adult and Pediatric Endocrinology, Diabetes andMetabolism is consistently recognized as one of the finest endocrinologycenters in the U.S. The University of Chicago\'s endocrinology programhas a reputation for progressive therapies and leading-edge research.The Kovler Diabetes Center is a globally renowned research hub and atreatment center of choice. The Center is...

　　Focused. Diabetes is all we do.

　　Patient centered. We empower our patients through treatment, educationand specialist access. The patient is our highest priority.

　　Comprehensive. Kovler encompasses research, patient care, professionaltraining, and patient education.

　　Science based. Evidence is the foundation of our treatment protocol. Wefocus on applied research to enhance patient care.

　　Multidisciplinary. Our team of specialists and educators addresses thefull range of patient needs, from the physical to the social andemotional.

　　To learn more, please visit:https://www.uchicagomedicine.org/conditions-services/diabetes

　　Job Summary

　　The Clinical Research Coordinator 2 provides support to the faculty ofthe Kovler Diabetes Center within the Biological Sciences Division. TheCRC 2 will be involved in multiple research trial types, such as:multi-centered cooperative group and intergroup studies at a nationallevel, multi-institutional pharmaceutical trials, and multi-centeredtrials designed, implemented and coordinated in the Center. This CRC 2will work primarily with the University of Chicago Monogenic DiabetesRegistry and related studies: https://monogenicdiabetes.uchicago.edu.

　　Responsibilities

　　Manages all aspects of conducting clinical trials including:screening, enrollment, subject follow-up, completion of the casereport form, and adverse event reports.Recruit and interview potential study patients with guidance from PIand other clinical research staff.Collect, process, ship and store specimens to appropriate laboratoryaccording to established aseptic techniques.Identify and explain the responsibilities of PrincipalInvestigators, research team members, sponsors, contract researchorganizations (CROs), and regulatory authorities related to theconduct of a clinical trial.Coordinate the conduct of the study from startup through closeoutincluding recruitment and screening of study subjects, obtaininginformed consent, collecting research data, and ensuring protocoladherence.Plans and coordinates patient schedule for study procedures, returnvisits, and study treatment schedules.Educates patients about study procedures to be performed, visitschedule, what to report between and during visits, and the risksand benefits of the procedures.Performs assessments at visits and monitors for adverse events.Organizes and attends site visits from sponsors and other relevantstudy meetings.Protect patients and data confidentiality by ensuring security ofresearch data and personal health information and compliance withfederal regulations and sponsor protocols.Ensures Standard Operating Procedures (SOP) are implemented anddocumented in accordance to study sponsor, primary investigator, andregulatory agency specifications.Maintains accurate and complete records which may include, but arenot limited to, signed informed consent, relevant IRB approvals,source document tion, Case Report Forms (CRF\'s), drug dispensinglogs, and study related communication.Understand the IRB submission and review process and when and how toapply for IRB review, including facilitation of study initiationthrough meticulous and timely preparation of IRB submissionsindependently.Ensures compliance with federal regulations and institutionalpolicies.May prepare and maintain protocol submissions and revisions.May assist in the training of new or backup coordinators.Coordinates and may participate in quality assurance reviewsconducted by study sponsors, federal agencies, or speciallydesignated review groups.Analyzes study-related documentation, such as protocol worksheets,procedural manuals, adverse event reports, institutional reviewboard documents, or progress reports.Performs other related work as needed.Minimum Qualifications

　　Education:

　　Minimum requirements include a college or university degree in relatedfield.

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　　Work Experience:

　　Minimum requirements include knowledge and skills developed through---

　　Certifications:

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　　Preferred Qualifications