University of Chicago
Clinical Research Coordinator 2, Trauma Surgery
University of Chicago, Chicago, Illinois, United States, 60290
Overview
Clinical Research Coordinator 2, Trauma Surgery at University of Chicago. The CRC2 is a specialized researcher working with the Principal Investigator, Co-Investigator(s) and study personnel. Under limited direction, the CRC2 supports administration of compliance, financial and other related aspects of the clinical study. Responsibilities
Research Conduct/Study Management: manages multiple moderately complex clinical trials, including recruitment and screening of study subjects, obtaining informed consent, enrollment, subject follow-up, data collection and analysis, completion of case report forms, adverse event reporting, and ensuring protocol adherence. Conducts sponsor-related visits and acts as liaison between sponsor and PI. Reviews study portfolio with PI; participates in study start-up activities; coordinates subject schedules and educates subjects about procedures, risks, and benefits; performs assessments and monitors for adverse events. Collects, processes, ships, and stores specimens per established aseptic techniques; identifies adverse events and deviations and reports findings to PI, sponsor, and IRB. Organizes site visits from sponsors and relevant study meetings; maintains safe research environment in compliance with policies and regulations. Data Management
Manages acquisition/collection, abstraction, processing, privacy, and quality assurance of clinical research data. Ensures data accuracy and integrity, supports source documentation, and coordinates data exchange across projects. Protects patient data confidentiality and PHI; ensures compliance with federal regulations and sponsor protocols. Ensures SOPs are implemented and documented per sponsor, PI, and regulatory specifications. Regulatory Compliance
Maintains records with Regulatory Manager (informed consent, IRB approvals, study communications) and ensures compliance with federal regulations and institutional policies. Mentors CRC1 or other staff on basic clinical research concepts, GCP, GDP, SOPs and related aspects. Other
Performs tasks under moderate supervision; supports daily activities of moderately complex studies, including data retrieval and audits; coordinates collection of analyzable data and/or samples; contributes to problem solving; performs other related work as needed. Education & Experience
Minimum Qualifications: college or university degree in a related field. Work Experience: 2-5 years in a related job discipline. Certifications: Preferred qualifications include continuing education such as ACRP, SoCRA, or the Graham School Clinical Trials. Preferred Qualifications & Competencies
Education: Bachelor’s degree; continuing education in clinical trials. Experience: Coordinating multiple studies (investigator-initiated, industry-sponsored, multi-site). Competencies: knowledge of patient evaluation and triage, clear communication, strong data management, protocol review ability, medical terminology, ability to handle competing demands, proficiency in Word/Excel/Adobe Acrobat, familiarity with GCP, understanding IRB process and federal regulations. Working Conditions
Occasional evening, night, and weekend work may be required to accommodate enrollment and data collection. Application Documents
Resume (required) Cover Letter (required) Apply documents via the My Experience page in the Application Documents section of the application. Pay & Benefits
Pay Range: $60,000.00 - $75,000.00 Benefits Eligible: Yes Equal Opportunity
The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or other protected classes. See the university’s Notice of Nondiscrimination for details.
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Clinical Research Coordinator 2, Trauma Surgery at University of Chicago. The CRC2 is a specialized researcher working with the Principal Investigator, Co-Investigator(s) and study personnel. Under limited direction, the CRC2 supports administration of compliance, financial and other related aspects of the clinical study. Responsibilities
Research Conduct/Study Management: manages multiple moderately complex clinical trials, including recruitment and screening of study subjects, obtaining informed consent, enrollment, subject follow-up, data collection and analysis, completion of case report forms, adverse event reporting, and ensuring protocol adherence. Conducts sponsor-related visits and acts as liaison between sponsor and PI. Reviews study portfolio with PI; participates in study start-up activities; coordinates subject schedules and educates subjects about procedures, risks, and benefits; performs assessments and monitors for adverse events. Collects, processes, ships, and stores specimens per established aseptic techniques; identifies adverse events and deviations and reports findings to PI, sponsor, and IRB. Organizes site visits from sponsors and relevant study meetings; maintains safe research environment in compliance with policies and regulations. Data Management
Manages acquisition/collection, abstraction, processing, privacy, and quality assurance of clinical research data. Ensures data accuracy and integrity, supports source documentation, and coordinates data exchange across projects. Protects patient data confidentiality and PHI; ensures compliance with federal regulations and sponsor protocols. Ensures SOPs are implemented and documented per sponsor, PI, and regulatory specifications. Regulatory Compliance
Maintains records with Regulatory Manager (informed consent, IRB approvals, study communications) and ensures compliance with federal regulations and institutional policies. Mentors CRC1 or other staff on basic clinical research concepts, GCP, GDP, SOPs and related aspects. Other
Performs tasks under moderate supervision; supports daily activities of moderately complex studies, including data retrieval and audits; coordinates collection of analyzable data and/or samples; contributes to problem solving; performs other related work as needed. Education & Experience
Minimum Qualifications: college or university degree in a related field. Work Experience: 2-5 years in a related job discipline. Certifications: Preferred qualifications include continuing education such as ACRP, SoCRA, or the Graham School Clinical Trials. Preferred Qualifications & Competencies
Education: Bachelor’s degree; continuing education in clinical trials. Experience: Coordinating multiple studies (investigator-initiated, industry-sponsored, multi-site). Competencies: knowledge of patient evaluation and triage, clear communication, strong data management, protocol review ability, medical terminology, ability to handle competing demands, proficiency in Word/Excel/Adobe Acrobat, familiarity with GCP, understanding IRB process and federal regulations. Working Conditions
Occasional evening, night, and weekend work may be required to accommodate enrollment and data collection. Application Documents
Resume (required) Cover Letter (required) Apply documents via the My Experience page in the Application Documents section of the application. Pay & Benefits
Pay Range: $60,000.00 - $75,000.00 Benefits Eligible: Yes Equal Opportunity
The University of Chicago is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or other protected classes. See the university’s Notice of Nondiscrimination for details.
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