The University Of Chicago
Clinical Research Coordinator 2
The University Of Chicago, Chicago, Illinois, United States, 60290
Clinical Research Coordinator 2
Clinical Research Coordinator 2 Apply remote type Hybrid locations Chicago, IL time type Full time posted on Posted 3 Days Ago job requisition id JR28795
Department
BSD PED - Clinical Trials Office: COG and HemOnc Research
About the Department
In the Department of Pediatrics at the University of Chicago, we strive to provide the highest level of complex care for children from diagnosis and treatment to conducting research to find promising new therapies with a focus on teaching. We are committed to advancing the frontiers of knowledge, and the education and training of future clinical pediatricians, subspecialists, educators, clinical investigators and physician-scientists.
The Pediatric Clinical Trials Office (Peds CTO) provides services and high-level guidance to individuals involved in human subjects research.
Job Summary
The Clinical Research Coordinator 2 (CRC2) provides support to the Section of Pediatric Hematology and Oncology. The CRC2 will be involved in multiple research trials types: investigator-initiated, multi-centered cooperative group studies, multi-institutional pharmaceutical trials, and multi-centered trials. The CRC2 supports, facilitates, and coordinates independently the daily clinical research activities.
Our department follows a hybrid work structure that fosters productivity, collaboration, and employee well-being. Working from the office is encouraged for tasks that require a high degree of collaboration.
Responsibilities
Analyzes, facilitates and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management.
Prepares program conference lists for multidisciplinary conferences and workshops.
Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study.
Manages all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
Collect, process, ship and store specimens to appropriate laboratory according to established aseptic techniques.
Coordinate 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.
Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and the risks and benefits of the procedures.
Protect patients and data confidentiality by ensuring security of research data and personal health information.
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 signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), and study related communication.
Ensures compliance with federal regulations and institutional policies.
May assist in the training of new or backup coordinators.
Analyzes 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.
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.
Preferred Qualifications
Education:
Bachelor’s degree.
Experience:
2 years of clinical research experience coordinating multiple and variety of studies.
Working Conditions
Eligible for hybrid work based on business needs and the demands of specific tasks.
Application Documents
Resume (required)
Cover Letter (required)
The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans employer. All offers of employment are contingent upon a background check that includes a review of conviction history.
The University of Chicago's Annual Security & Fire Safety Report provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online
#J-18808-Ljbffr
Clinical Research Coordinator 2 Apply remote type Hybrid locations Chicago, IL time type Full time posted on Posted 3 Days Ago job requisition id JR28795
Department
BSD PED - Clinical Trials Office: COG and HemOnc Research
About the Department
In the Department of Pediatrics at the University of Chicago, we strive to provide the highest level of complex care for children from diagnosis and treatment to conducting research to find promising new therapies with a focus on teaching. We are committed to advancing the frontiers of knowledge, and the education and training of future clinical pediatricians, subspecialists, educators, clinical investigators and physician-scientists.
The Pediatric Clinical Trials Office (Peds CTO) provides services and high-level guidance to individuals involved in human subjects research.
Job Summary
The Clinical Research Coordinator 2 (CRC2) provides support to the Section of Pediatric Hematology and Oncology. The CRC2 will be involved in multiple research trials types: investigator-initiated, multi-centered cooperative group studies, multi-institutional pharmaceutical trials, and multi-centered trials. The CRC2 supports, facilitates, and coordinates independently the daily clinical research activities.
Our department follows a hybrid work structure that fosters productivity, collaboration, and employee well-being. Working from the office is encouraged for tasks that require a high degree of collaboration.
Responsibilities
Analyzes, facilitates and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management.
Prepares program conference lists for multidisciplinary conferences and workshops.
Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study.
Manages all aspects of conducting clinical trials including: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
Collect, process, ship and store specimens to appropriate laboratory according to established aseptic techniques.
Coordinate 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.
Educates patients about study procedures to be performed, visit schedule, what to report between and during visits, and the risks and benefits of the procedures.
Protect patients and data confidentiality by ensuring security of research data and personal health information.
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 signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), and study related communication.
Ensures compliance with federal regulations and institutional policies.
May assist in the training of new or backup coordinators.
Analyzes 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.
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.
Preferred Qualifications
Education:
Bachelor’s degree.
Experience:
2 years of clinical research experience coordinating multiple and variety of studies.
Working Conditions
Eligible for hybrid work based on business needs and the demands of specific tasks.
Application Documents
Resume (required)
Cover Letter (required)
The University of Chicago is an Affirmative Action/Equal Opportunity/Disabled/Veterans employer. All offers of employment are contingent upon a background check that includes a review of conviction history.
The University of Chicago's Annual Security & Fire Safety Report provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information. The Report can be accessed online
#J-18808-Ljbffr