University of Chicago
Clinical Research Coordinator 2
University of Chicago, Chicago, Illinois, United States, 60290
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Clinical Research Coordinator 2
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Clinical Research Coordinator 2
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University of Chicago Get AI-powered advice on this job and more exclusive features. About The Department
Department
BSD NEU - Clinical Research Staff
About The Department
The Department of Neurology at The University of Chicago Medical Center has a great history and tradition, having made significant contributions to neurological training, clinical care, and the basic understanding of neurological disease. This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the contract.
Job Summary
The Clinical Research Coordinator 2 will perform routine assignments related to the documentation, analysis, and reporting of research data within the Department of Neurology.
Responsibilities
Conducts site qualifications, study initiation, monitoring and/or close-out visits. Conducts study start-up activities and works in collaboration with regulatory manager to maintain all regulatory documents required by sponsor and/or regulatory agencies. Coordinates study conduct with other departments to effectively implement clinical research projects; ensures all study trainings are completed by study team; obtains required letters of support and/or approvals as needed. Identifies and recruits eligible study subjects; conducts informed consent/assent process. Arranges and conducts clinical research visits. Abstracts data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms; prepares abstracted/coded data for processing/analysis. Creates and/or updates case report form and/or source document templates. Coordinates reimbursement of subjects. Maintains inventory of supplies/equipment. Collects specimens from subjects and processes specimens or works with lab to ensure samples are processed/sent out correctly. Monitors/assesses adverse events and reports them as required. Adheres to research protocol in compliance with applicable institutional, local and federal regulations (FDA, GCP, etc.). Functions as patient liaison for study questions, billing issues, etc. Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups. Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits. Accountable for all tasks in moderately complex clinical studies. Performs other related work as needed.
Education:
Minimum Qualifications
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 Qualifications
Education:
Bachelors degree.
Experience:
Clinical research experience or relevant experience. Experience coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials).
Preferred Competencies
Aware of safety hazards and take appropriate precautions. Communicate in writing. Communicate orally. Comprehend technical documents. Condense complicated issues to simple summaries that can be understood by a variety of constituents. Create and deliver presentations. Develop and manage interpersonal relationships. Exercise absolute discretion regarding confidential matters. Follow written and/or verbal instructions. Give directions. Handle sensitive matters with tact and discretion. Handle stressful situations. Learn and develop skills. Maintain a high level of alertness. Pay attention to detail. Perform multiple tasks simultaneously. Prioritize work and meet deadlines. React effectively, quickly, calmly, and rationally during conflicts and emergencies. Train or teach others. Work effectively and collegially with little supervision or as member of a team. Work independently.
Application Documents
Resume/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
Research
Role Impact
Individual Contributor
Scheduled
Weekly Hours
40
Drug Test Required
Yes
Health Screen Required
Yes
Motor Vehicle Record Inquiry Required
No
Pay Rate Type
Salary
FLSA Status
Exempt
Pay Range
$60,000.00 - $75,000.00
The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.
Benefits Eligible
Yes
The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.
Posting Statement
The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, 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.
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.
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. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Other Job function
Job function Research, Analyst, and Information Technology Industries Higher Education Referrals increase your chances of interviewing at University of Chicago by 2x Sign in to set job alerts for “Clinical Research Coordinator” roles.
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Clinical Research Coordinator 2
role at
University of Chicago 1 month ago Be among the first 25 applicants Join to apply for the
Clinical Research Coordinator 2
role at
University of Chicago Get AI-powered advice on this job and more exclusive features. About The Department
Department
BSD NEU - Clinical Research Staff
About The Department
The Department of Neurology at The University of Chicago Medical Center has a great history and tradition, having made significant contributions to neurological training, clinical care, and the basic understanding of neurological disease. This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the contract.
Job Summary
The Clinical Research Coordinator 2 will perform routine assignments related to the documentation, analysis, and reporting of research data within the Department of Neurology.
Responsibilities
Conducts site qualifications, study initiation, monitoring and/or close-out visits. Conducts study start-up activities and works in collaboration with regulatory manager to maintain all regulatory documents required by sponsor and/or regulatory agencies. Coordinates study conduct with other departments to effectively implement clinical research projects; ensures all study trainings are completed by study team; obtains required letters of support and/or approvals as needed. Identifies and recruits eligible study subjects; conducts informed consent/assent process. Arranges and conducts clinical research visits. Abstracts data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms; prepares abstracted/coded data for processing/analysis. Creates and/or updates case report form and/or source document templates. Coordinates reimbursement of subjects. Maintains inventory of supplies/equipment. Collects specimens from subjects and processes specimens or works with lab to ensure samples are processed/sent out correctly. Monitors/assesses adverse events and reports them as required. Adheres to research protocol in compliance with applicable institutional, local and federal regulations (FDA, GCP, etc.). Functions as patient liaison for study questions, billing issues, etc. Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups. Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits. Accountable for all tasks in moderately complex clinical studies. Performs other related work as needed.
Education:
Minimum Qualifications
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 Qualifications
Education:
Bachelors degree.
Experience:
Clinical research experience or relevant experience. Experience coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials).
Preferred Competencies
Aware of safety hazards and take appropriate precautions. Communicate in writing. Communicate orally. Comprehend technical documents. Condense complicated issues to simple summaries that can be understood by a variety of constituents. Create and deliver presentations. Develop and manage interpersonal relationships. Exercise absolute discretion regarding confidential matters. Follow written and/or verbal instructions. Give directions. Handle sensitive matters with tact and discretion. Handle stressful situations. Learn and develop skills. Maintain a high level of alertness. Pay attention to detail. Perform multiple tasks simultaneously. Prioritize work and meet deadlines. React effectively, quickly, calmly, and rationally during conflicts and emergencies. Train or teach others. Work effectively and collegially with little supervision or as member of a team. Work independently.
Application Documents
Resume/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
Research
Role Impact
Individual Contributor
Scheduled
Weekly Hours
40
Drug Test Required
Yes
Health Screen Required
Yes
Motor Vehicle Record Inquiry Required
No
Pay Rate Type
Salary
FLSA Status
Exempt
Pay Range
$60,000.00 - $75,000.00
The included pay rate or range represents the University’s good faith estimate of the possible compensation offer for this role at the time of posting.
Benefits Eligible
Yes
The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off. Information about the benefit offerings can be found in the Benefits Guidebook.
Posting Statement
The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender, gender identity, or expression, national or ethnic origin, shared ancestry, 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.
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.
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. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Other Job function
Job function Research, Analyst, and Information Technology Industries Higher Education Referrals increase your chances of interviewing at University of Chicago by 2x Sign in to set job alerts for “Clinical Research Coordinator” roles.
Chicago, IL $64,015.00-$74,523.00 8 months ago Streeterville, IL $59,280.00-$96,928.00 1 month ago Clinical Research Coordinator I- Neonatology
Part Time - Clinical Robot Associate - Chicago, IL
Clinical Research Coordinator 1 – Pediatrics
Chicago, IL $50,000.00-$65,000.00 2 months ago Chicago, IL $50,000.00-$65,000.00 2 months ago Clinical Research Coordinator 1 – Pediatrics
Clinical Research Coordinator I - Neonatology
Clinical Research Coordinator 1 – Pediatrics
Chicago, IL $52,000.00-$65,000.00 2 months ago Chicago, IL $51,346.00-$64,473.00 1 week ago Chicago, IL $55,000.00-$70,000.00 2 months ago Chicago, IL $60,000.00-$75,000.00 2 months ago Clinical Research Coordinator 1 – Pediatrics
Chicago, IL $50,000.00-$65,000.00 2 months ago Clinical Research Coordinator 1 – Pediatrics
Chicago, IL $50,000.00-$65,000.00 2 months ago Chicago, IL $70,000.00-$80,000.00 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr