University of Chicago
Clinical Research Coordinator 2
University of Chicago, Chicago, Illinois, United States, 60290
Overview
Clinical Research Coordinator 2 (CRC2) position at the University of Chicago. The CRC2 is a specialized researcher who partners with the clinical Principal Investigator (PI) and supports daily clinical trial activities under supervision, coordinating compliance, financial, personnel, and other aspects of the study. Base pay range
$60,000.00/yr - $75,000.00/yr Department context
BSD MED - Hematology and Oncology - Clinical Research Staff - Cluster 7. The Section of Hematology/Oncology conducts research-based patient care and clinical discovery with expertise across major malignancies, blood disorders, and experimental therapies. Responsibilities
Manage all aspects of conducting clinical trials including screening, enrollment, subject follow-up, case report forms, and adverse event reports. Recruit and interview potential study patients with guidance from the PI and clinical research staff. Collect, process, ship, and store specimens per established aseptic techniques. Explain roles and responsibilities of investigators, sponsors, CROs, and regulatory authorities related to the trial. Coordinate study startup through closeout, including informed consent, data collection, and protocol adherence. Plan and coordinate patient schedules for procedures, visits, and treatment timelines. Educate patients about procedures, visit schedules, reporting requirements, and risks/benefits. Perform assessments at visits and monitor adverse events. Organize site visits from sponsors and other study meetings. Protect patient and data confidentiality and ensure compliance with federal regulations and sponsor protocols. Ensure SOPs are implemented and documented per sponsor, PI, and regulatory agency specifications. Maintain accurate records (informed consent, IRB approvals, source documentation, CRFs, drug dispensing logs, communications). Understand IRB submission and review processes; facilitate study initiation and timely IRB submissions. Ensure compliance with federal regulations and institutional policies. Assist in training of new or backup coordinators. Contribute to daily activities of moderately complex clinical trials, including data management and audits. Address straightforward problems related to compliance, financial, and related aspects of the study. Participate in daily activities of moderately complex studies and document research records. Accountable for all tasks in moderately complex studies. Performs other related work as needed. Minimum qualifications
Education:
A college or university degree in a related field. Work Experience:
2-5 years of related work experience. Preferred qualifications
Clinical research experience or relevant experience. Experience coordinating multiple studies (investigator-initiated, industry-sponsored, multi-site). Technical skills
Understand safety hazards and take appropriate precautions. Ability to comprehend technical documents and communicate clearly in writing and verbally. Develop and manage interpersonal relationships; follow instructions; handle sensitive matters with tact. Train others; work independently or with minimal supervision; meet deadlines; manage conflicts and emergencies. Application documents
Resume/CV (required) When applying, upload documents via the My Experience page in the Application Documents section. Job details
Job family: Research Role impact: standard Scheduled Weekly Hours: 37.5 Drug Test Required: Yes Health Screen Required: Yes Motor Vehicle Record Inquiry Required: No Pay Rate Type: Salary FLSA Status: Exempt Benefits Eligible: Yes Posting Statement: The University of Chicago is an equal opportunity employer and does not discriminate on the basis of protected characteristics. Reasonable accommodation requests: 773-702-5800 or Applicant Inquiry Form. Background check required for offers. Seniority level
Associate Employment type
Full-time Job function
Research, Health Care Provider, and Science Industries
Higher Education Hospitals and Health Care Education Get notified about new Clinical Research Coordinator jobs in Chicago, IL.
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Clinical Research Coordinator 2 (CRC2) position at the University of Chicago. The CRC2 is a specialized researcher who partners with the clinical Principal Investigator (PI) and supports daily clinical trial activities under supervision, coordinating compliance, financial, personnel, and other aspects of the study. Base pay range
$60,000.00/yr - $75,000.00/yr Department context
BSD MED - Hematology and Oncology - Clinical Research Staff - Cluster 7. The Section of Hematology/Oncology conducts research-based patient care and clinical discovery with expertise across major malignancies, blood disorders, and experimental therapies. Responsibilities
Manage all aspects of conducting clinical trials including screening, enrollment, subject follow-up, case report forms, and adverse event reports. Recruit and interview potential study patients with guidance from the PI and clinical research staff. Collect, process, ship, and store specimens per established aseptic techniques. Explain roles and responsibilities of investigators, sponsors, CROs, and regulatory authorities related to the trial. Coordinate study startup through closeout, including informed consent, data collection, and protocol adherence. Plan and coordinate patient schedules for procedures, visits, and treatment timelines. Educate patients about procedures, visit schedules, reporting requirements, and risks/benefits. Perform assessments at visits and monitor adverse events. Organize site visits from sponsors and other study meetings. Protect patient and data confidentiality and ensure compliance with federal regulations and sponsor protocols. Ensure SOPs are implemented and documented per sponsor, PI, and regulatory agency specifications. Maintain accurate records (informed consent, IRB approvals, source documentation, CRFs, drug dispensing logs, communications). Understand IRB submission and review processes; facilitate study initiation and timely IRB submissions. Ensure compliance with federal regulations and institutional policies. Assist in training of new or backup coordinators. Contribute to daily activities of moderately complex clinical trials, including data management and audits. Address straightforward problems related to compliance, financial, and related aspects of the study. Participate in daily activities of moderately complex studies and document research records. Accountable for all tasks in moderately complex studies. Performs other related work as needed. Minimum qualifications
Education:
A college or university degree in a related field. Work Experience:
2-5 years of related work experience. Preferred qualifications
Clinical research experience or relevant experience. Experience coordinating multiple studies (investigator-initiated, industry-sponsored, multi-site). Technical skills
Understand safety hazards and take appropriate precautions. Ability to comprehend technical documents and communicate clearly in writing and verbally. Develop and manage interpersonal relationships; follow instructions; handle sensitive matters with tact. Train others; work independently or with minimal supervision; meet deadlines; manage conflicts and emergencies. Application documents
Resume/CV (required) When applying, upload documents via the My Experience page in the Application Documents section. Job details
Job family: Research Role impact: standard Scheduled Weekly Hours: 37.5 Drug Test Required: Yes Health Screen Required: Yes Motor Vehicle Record Inquiry Required: No Pay Rate Type: Salary FLSA Status: Exempt Benefits Eligible: Yes Posting Statement: The University of Chicago is an equal opportunity employer and does not discriminate on the basis of protected characteristics. Reasonable accommodation requests: 773-702-5800 or Applicant Inquiry Form. Background check required for offers. Seniority level
Associate Employment type
Full-time Job function
Research, Health Care Provider, and Science Industries
Higher Education Hospitals and Health Care Education Get notified about new Clinical Research Coordinator jobs in Chicago, IL.
#J-18808-Ljbffr