The University of Chicago
Clinical Research Coordinator
The University of Chicago, Chicago, Illinois, United States, 60290
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Clinical Research Coordinator
Apply remote type Onsite locations Chicago, IL time type Full time posted on Posted 3 Days Ago job requisition id JR31310
Department BSD RAO - Operations About the Department The Department of Radiation and Cellular Oncology at the University of Chicago is renowned for advancing the field of radiation oncology through pioneering new clinical approaches, the use of cutting-edge technologies, and impactful translational research. Our distinguished and diverse team of physicians, scientists, and physicists collaboratively provide exceptional patient care while driving scientific discoveries that shape the future of cancer treatment. Job Summary The Clinical Research Coordinator supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study. This position offers you the opportunity to lead patient recruitment, coordinate study visits, and conduct informed consent discussions while ensuring protocol adherence and patient safety. The Clinical Research Coordinator will oversee specimen handling, perform study assessments, manage case report forms and adverse event documentation, and safeguard patient data. In addition, this position will liaise with principal investigators, sponsors, CROs, and regulatory bodies, and prepare and maintain IRB submissions and approvals.
Responsibilities Plays a central role in managing all aspects of clinical trials from start-up through close-out.
Lead patient recruitment, coordinate study visits, and conduct informed consent discussions while ensuring protocol adherence and patient safety.
Oversee specimen handling, perform study assessments, manage case report forms and adverse event documentation, and safeguard patient data with meticulous attention to confidentiality and compliance.
Liaise with principal investigators, sponsors, CROs, and regulatory bodies, and prepare and maintain IRB submissions and approvals.
Training new staff, participating in audits, resolving logistical and administrative challenges, and maintaining detailed research records.
Accountable for all tasks in basic clinical studies.
Assists with various professional, organizational, and operational tasks under direct supervision.
Supports quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
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 Certifications: --- Preferred Qualifications Experience: Experience in conducting oncology trials and research.
Working Conditions Clinical Environment.
Application Documents Resume (required)
Cover Letter (preferred)
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 $50,000.00 - $65,000.00
The included pay rate or range represents the Universitys 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 theBenefits 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. Similar Jobs (3)
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Apply remote type Onsite locations Chicago, IL time type Full time posted on Posted 3 Days Ago job requisition id JR31310
Department BSD RAO - Operations About the Department The Department of Radiation and Cellular Oncology at the University of Chicago is renowned for advancing the field of radiation oncology through pioneering new clinical approaches, the use of cutting-edge technologies, and impactful translational research. Our distinguished and diverse team of physicians, scientists, and physicists collaboratively provide exceptional patient care while driving scientific discoveries that shape the future of cancer treatment. Job Summary The Clinical Research Coordinator supports, facilitates and coordinates independently the daily clinical trial activities and plays a critical role in the conduct of the study. This position offers you the opportunity to lead patient recruitment, coordinate study visits, and conduct informed consent discussions while ensuring protocol adherence and patient safety. The Clinical Research Coordinator will oversee specimen handling, perform study assessments, manage case report forms and adverse event documentation, and safeguard patient data. In addition, this position will liaise with principal investigators, sponsors, CROs, and regulatory bodies, and prepare and maintain IRB submissions and approvals.
Responsibilities Plays a central role in managing all aspects of clinical trials from start-up through close-out.
Lead patient recruitment, coordinate study visits, and conduct informed consent discussions while ensuring protocol adherence and patient safety.
Oversee specimen handling, perform study assessments, manage case report forms and adverse event documentation, and safeguard patient data with meticulous attention to confidentiality and compliance.
Liaise with principal investigators, sponsors, CROs, and regulatory bodies, and prepare and maintain IRB submissions and approvals.
Training new staff, participating in audits, resolving logistical and administrative challenges, and maintaining detailed research records.
Accountable for all tasks in basic clinical studies.
Assists with various professional, organizational, and operational tasks under direct supervision.
Supports quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
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 Certifications: --- Preferred Qualifications Experience: Experience in conducting oncology trials and research.
Working Conditions Clinical Environment.
Application Documents Resume (required)
Cover Letter (preferred)
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 $50,000.00 - $65,000.00
The included pay rate or range represents the Universitys 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 theBenefits 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. Similar Jobs (3)
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