The University Of Chicago
Clinical Research Coordinator 2
The University Of Chicago, Chicago, Illinois, United States, 60290
Clinical Research Coordinator 2 page is loaded
Clinical Research Coordinator 2
Apply
locations
Chicago, IL
time type
Full time
posted on
Posted 30+ Days Ago
job requisition id
JR26042
Department
BSD MED - Pulmonary - Tasali Research StaffAbout the Department
The UChicago Medicine Sleep Center is a fully integrated center of excellence for sleep and health. Our sleep experts provide and support patient care, education and research. The center aims to foster growth, collaboration and success in diverse areas of science and medicine at both the national and international levels.Job Summary
The Clinical Research Coordinator 2 (CRC) works under the direction of the Principal Investigator (PI) and in combination with other lab personnel. The CRC supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC performs social-behavioral research by administering tests and/or questionnaires; following protocols; collecting, compiling, and processing responses; gathering information; and/or assisting in the preparation of material for inclusion in reports. The CRC2 will be assigned to a new study protocol: 'Effect of early parent education on children’s sleep: beyond risk factors.' The study seeks to investigate how parents’ behaviors affect infant sleep and the influence behind such behaviors. Participating parents with infants will be randomized into one of two groups: General Sleep Information or General Plus Detailed Sleep Information. Study participation will last 24 months. Data will be collected on parents’ and infants’ backgrounds and sleep-related behaviors. The CRC2 will be responsible for preparation of study protocol and materials, study initiation, communication with IRB, and day to day coordination of participant enrollment and data collection.
ResponsibilitiesPrepares study protocol for IRB review.
Communicates with IRB throughout study to maintain study approval.
Develops data collection materials.
Coordinates the study from startup through closeout.
Consults with nurses and physicians to determine eligibility requirements of participants.
Recruits study participants.
Reviews and obtains informed consent.
Schedules study visits with participants.
Conducts interviews.
Scores test results.
Collects, extracts, and enters data.
Monitors and distribute compensation to participants.
Facilitates communication with personnel and participants to maintain project study flow.
Maintains detailed records of results.
Prepares basic charts and graphs.
Performs scientific literature searches in support of research being conducted.
Processes invoices and/or purchase requisitions.
May train other research staff to interview participants.
Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study.
Interprets the data needed for insurance submissions. Gathers pre-testing results if obtained at an outside facility.
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 QualificationsEducation:Bachelor's degree.
Experience:Experience with clinical study initiation.
Experience with IRB (Good Clinical Practice certification, comfortable communicating with study monitors, knowledge on IRB submission, review, and approval).
Experience working with human research subjects, ideally in the field of sleep, pediatrics, or family medicine.
Knowledge or experience with REDCap.
Experience with primary data entry and analysis (REDCap, Excel, JMP).
Preferred CompetenciesDetail oriented and able to work independently.
Communicate in writing.
Communicate orally.
Comprehend technical documents.
Pay attention to detail.
Perform multiple tasks simultaneously.
Prioritize work and meet deadlines.
Handle sensitive matters with tact and discretion.
Application DocumentsResume/CV (required)
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.
Job Family
ResearchRole Impact
Individual ContributorFLSA Status
ExemptPay Frequency
MonthlyScheduled
Weekly Hours
40Benefits Eligible
YesDrug Test Required
YesHealth Screen Required
YesMotor Vehicle Record Inquiry Required
NoPosting Statement
The University of Chicago is an Affirmative Action/Equal
Opportunity/Disabled/Veterans
and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, national or ethnic origin, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the
University's Notice of Nondiscrimination.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.All offers of employment are contingent upon a background check that includes a review of conviction history.A conviction does not automatically preclude University employment.Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.The University of Chicago's Annual Security & Fire Safety Report (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 at:
http://securityreport.uchicago.edu
. Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.Similar Jobs (6)
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#J-18808-Ljbffr
Clinical Research Coordinator 2
Apply
locations
Chicago, IL
time type
Full time
posted on
Posted 30+ Days Ago
job requisition id
JR26042
Department
BSD MED - Pulmonary - Tasali Research StaffAbout the Department
The UChicago Medicine Sleep Center is a fully integrated center of excellence for sleep and health. Our sleep experts provide and support patient care, education and research. The center aims to foster growth, collaboration and success in diverse areas of science and medicine at both the national and international levels.Job Summary
The Clinical Research Coordinator 2 (CRC) works under the direction of the Principal Investigator (PI) and in combination with other lab personnel. The CRC supports, facilitates, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC performs social-behavioral research by administering tests and/or questionnaires; following protocols; collecting, compiling, and processing responses; gathering information; and/or assisting in the preparation of material for inclusion in reports. The CRC2 will be assigned to a new study protocol: 'Effect of early parent education on children’s sleep: beyond risk factors.' The study seeks to investigate how parents’ behaviors affect infant sleep and the influence behind such behaviors. Participating parents with infants will be randomized into one of two groups: General Sleep Information or General Plus Detailed Sleep Information. Study participation will last 24 months. Data will be collected on parents’ and infants’ backgrounds and sleep-related behaviors. The CRC2 will be responsible for preparation of study protocol and materials, study initiation, communication with IRB, and day to day coordination of participant enrollment and data collection.
ResponsibilitiesPrepares study protocol for IRB review.
Communicates with IRB throughout study to maintain study approval.
Develops data collection materials.
Coordinates the study from startup through closeout.
Consults with nurses and physicians to determine eligibility requirements of participants.
Recruits study participants.
Reviews and obtains informed consent.
Schedules study visits with participants.
Conducts interviews.
Scores test results.
Collects, extracts, and enters data.
Monitors and distribute compensation to participants.
Facilitates communication with personnel and participants to maintain project study flow.
Maintains detailed records of results.
Prepares basic charts and graphs.
Performs scientific literature searches in support of research being conducted.
Processes invoices and/or purchase requisitions.
May train other research staff to interview participants.
Solves a range of straightforward problems relating to the administration of the compliance, financial and other related aspects of a clinical study.
Interprets the data needed for insurance submissions. Gathers pre-testing results if obtained at an outside facility.
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 QualificationsEducation:Bachelor's degree.
Experience:Experience with clinical study initiation.
Experience with IRB (Good Clinical Practice certification, comfortable communicating with study monitors, knowledge on IRB submission, review, and approval).
Experience working with human research subjects, ideally in the field of sleep, pediatrics, or family medicine.
Knowledge or experience with REDCap.
Experience with primary data entry and analysis (REDCap, Excel, JMP).
Preferred CompetenciesDetail oriented and able to work independently.
Communicate in writing.
Communicate orally.
Comprehend technical documents.
Pay attention to detail.
Perform multiple tasks simultaneously.
Prioritize work and meet deadlines.
Handle sensitive matters with tact and discretion.
Application DocumentsResume/CV (required)
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.
Job Family
ResearchRole Impact
Individual ContributorFLSA Status
ExemptPay Frequency
MonthlyScheduled
Weekly Hours
40Benefits Eligible
YesDrug Test Required
YesHealth Screen Required
YesMotor Vehicle Record Inquiry Required
NoPosting Statement
The University of Chicago is an Affirmative Action/Equal
Opportunity/Disabled/Veterans
and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, national or ethnic origin, age, status as an individual with a disability, military or veteran status, genetic information, or other protected classes under the law. For additional information please see the
University's Notice of Nondiscrimination.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.All offers of employment are contingent upon a background check that includes a review of conviction history.A conviction does not automatically preclude University employment.Rather, the University considers conviction information on a case-by-case basis and assesses the nature of the offense, the circumstances surrounding it, the proximity in time of the conviction, and its relevance to the position.The University of Chicago's Annual Security & Fire Safety Report (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 at:
http://securityreport.uchicago.edu
. Paper copies of the Report are available, upon request, from the University of Chicago Police Department, 850 E. 61st Street, Chicago, IL 60637.Similar Jobs (6)
Clinical Research Coordinator 2
locations
Chicago, IL
time type
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posted on
Posted 30+ Days Ago
Senior Qualitative Research Analyst
locations
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time type
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posted on
Posted 30+ Days Ago
Clinical Research Coordinator 2
locations
Chicago, IL
time type
Full time
posted on
Posted 30+ Days AgoThe University of Chicago is an urban research university that has driven new ways of thinking since 1890. Our commitment to free and open inquiry draws inspired scholars to our global campuses, where ideas are born that challenge and change the world.We empower individuals to challenge conventional thinking in pursuit of original ideas. Students in the College develop critical, analytic, and writing skills in our rigorous, interdisciplinary core curriculum. Through graduate programs, students test their ideas with UChicago scholars, and become the next generation of leaders in academia, industry, nonprofits, and government.
#J-18808-Ljbffr