The University of Chicago
Clinical Research Nurse Coordinator
The University of Chicago, Chicago, Illinois, United States, 60290
This job was posted by https://illinoisjoblink.illinois.gov : For more information, please see: https://illinoisjoblink.illinois.gov/jobs/12311913 Department
BSD IPP - Clinical Research
About the Department
The Institute for Population and Precision Health (IPPH), located in the Biological Sciences Division, integrates a wide spectrum of factors such as human health behaviors, environmental factors, social and economic factors, policies and genetic determinants of health, into studies focused on the treatment and prevention of disease, as well as the maintenance of wellness. Leveraging and integrating the University of Chicago\'s considerable institutional strength in population science with research spanning diverse fields such as genetic medicine, cancer epidemiology, microbiome, and epigenomics, the Institute will have the common goal of improving human health outcomes. Another major goal of the Institute will be to develop a new multidisciplinary training program to equip researchers with emerging tools and methods to conduct precision health research within a population health framework. Our faculty lead research projects in biostatistics, epidemiology and health services research and participate in interdisciplinary teams with faculty in other departments to address complex problems in health and healthcare, in our communities and around the globe.
Job Summary
The job provides professional support and solves straightforward problems in nursing assist in the design, development, and ongoing modification of health care to patients. May educate staff and assist in problem solving to promote the implementation of the health care system.
Responsibilities
Coordinate and participate in the conduct of clinical research trials at the Institute for Population and Precision Health (IPPH).Assist with or plan and implement the clinical study\'s goals and objectives; organize patient enrollment planning; conduct quality assurance activities, compile and analyze data.Develop and implement study procedures, maintains study records, tracks study progress, and conducts quality assurance on study data collected.Prepare, submit, and assist investigators with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms).Provide direct supervision of other research staff (i.e. hiring/firing, performance evaluations, disciplinary actions, approve time off, etc.), or assist.Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities.Conduct clinical study tasks including physical assessment of subjects, taking vital signs, recording medical, surgical, social and behavioral histories, and phlebotomy skills.Serve as a resource person or act as a consultant within area of clinical expertise.Act as a leader within the department/unit through improving clinical research practice and serving as a resource.Maintain working knowledge of current protocols, and internal SOPs.Be accountable for high standards of clinical research practice and assist in the development of accountability in others.Oversee and participate in the coordination and conduct of complex clinical research studies and ensure compliance with study standard operating protocols and procedures as well as federal and institutional regulations.Provide Investigators with guidance regarding protocol requirements.Maintain regulatory documentation.Assist other research personnel with reports to regulatory agencies, such as the IRB, FDA and Data and Safety Review Committee.Prepare for and assist with audits, inspections, and monitoring visits from regulatory agencies or sponsors.Applies logic and reasoning to identi y the strengths and weaknesses of alternative solutions, conclusions or approaches to problems.Interprets information from caregivers, nurses, or physicians about patient condition, treatment plans, or appropriate activities.Has a solid understanding of the information and techniques needed to diagnose and treat human injuries, diseases, and deformities. This includes symptoms, treatment alternatives, drug properties and interactions, and preventive health-care measures.Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
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Work Experience:
Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
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Certifications:
---
Preferred Competencies
Research certification (e.g., SoCRA, ACRP, Graham School Clinical Trials Management & Regulatory Compliance).
Fundamental working knowledge of clinical research.
Knowledge of clinical trials regulatory requirements.
Knowledge of patient care fund
BSD IPP - Clinical Research
About the Department
The Institute for Population and Precision Health (IPPH), located in the Biological Sciences Division, integrates a wide spectrum of factors such as human health behaviors, environmental factors, social and economic factors, policies and genetic determinants of health, into studies focused on the treatment and prevention of disease, as well as the maintenance of wellness. Leveraging and integrating the University of Chicago\'s considerable institutional strength in population science with research spanning diverse fields such as genetic medicine, cancer epidemiology, microbiome, and epigenomics, the Institute will have the common goal of improving human health outcomes. Another major goal of the Institute will be to develop a new multidisciplinary training program to equip researchers with emerging tools and methods to conduct precision health research within a population health framework. Our faculty lead research projects in biostatistics, epidemiology and health services research and participate in interdisciplinary teams with faculty in other departments to address complex problems in health and healthcare, in our communities and around the globe.
Job Summary
The job provides professional support and solves straightforward problems in nursing assist in the design, development, and ongoing modification of health care to patients. May educate staff and assist in problem solving to promote the implementation of the health care system.
Responsibilities
Coordinate and participate in the conduct of clinical research trials at the Institute for Population and Precision Health (IPPH).Assist with or plan and implement the clinical study\'s goals and objectives; organize patient enrollment planning; conduct quality assurance activities, compile and analyze data.Develop and implement study procedures, maintains study records, tracks study progress, and conducts quality assurance on study data collected.Prepare, submit, and assist investigators with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant renewal reports, and study forms).Provide direct supervision of other research staff (i.e. hiring/firing, performance evaluations, disciplinary actions, approve time off, etc.), or assist.Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities.Conduct clinical study tasks including physical assessment of subjects, taking vital signs, recording medical, surgical, social and behavioral histories, and phlebotomy skills.Serve as a resource person or act as a consultant within area of clinical expertise.Act as a leader within the department/unit through improving clinical research practice and serving as a resource.Maintain working knowledge of current protocols, and internal SOPs.Be accountable for high standards of clinical research practice and assist in the development of accountability in others.Oversee and participate in the coordination and conduct of complex clinical research studies and ensure compliance with study standard operating protocols and procedures as well as federal and institutional regulations.Provide Investigators with guidance regarding protocol requirements.Maintain regulatory documentation.Assist other research personnel with reports to regulatory agencies, such as the IRB, FDA and Data and Safety Review Committee.Prepare for and assist with audits, inspections, and monitoring visits from regulatory agencies or sponsors.Applies logic and reasoning to identi y the strengths and weaknesses of alternative solutions, conclusions or approaches to problems.Interprets information from caregivers, nurses, or physicians about patient condition, treatment plans, or appropriate activities.Has a solid understanding of the information and techniques needed to diagnose and treat human injuries, diseases, and deformities. This includes symptoms, treatment alternatives, drug properties and interactions, and preventive health-care measures.Performs other related work as needed.
Minimum Qualifications
Education:
Minimum requirements include a college or university degree in related field.
---
Work Experience:
Minimum requirements include knowledge and skills developed through 2-5 years of work experience in a related job discipline.
---
Certifications:
---
Preferred Competencies
Research certification (e.g., SoCRA, ACRP, Graham School Clinical Trials Management & Regulatory Compliance).
Fundamental working knowledge of clinical research.
Knowledge of clinical trials regulatory requirements.
Knowledge of patient care fund