Rush University Medical Center
Clinical Research Coordinator I-22430
Rush University Medical Center, Chicago, Illinois, United States, 60290
Application for
Clinical Research Coordinator I-22430
at
Rush University Medical Center , Chicago, Illinois.
Job Summary The Clinical Research Coordinator I (CRC I) supports the conduct of clinical research studies across a range of disciplines. The CRC I receives direction from the principal investigator or supervisor and is responsible for participant recruitment and interaction, study data collection and entry, maintenance of study and regulatory documentation, sponsor communication, and adherence to study protocols and policies. The CRC I executes defined study tasks with guidance, ensuring operational compliance, accurate data entry, and participant safety.
Education Bachelor’s degree
Required Experience
0–2 years of experience in a research study or other relevant experience
OR, Two (2) years’ total experience, where 1 year is supporting or coordinating research studies
Preferred Experience Two (2) or more years prior experience in clinical research or related field
Knowledge, Skills, & Abilities
Time Management – Ability to meet deadlines and manage assigned study tasks.
Problem‑Solving – Ability to troubleshoot routine field issues and use discretion to elevate appropriately when unplanned events arise.
Attention to Detail – Strong attention to accuracy in data collection and documentation.
Participant Relations – Ability to build rapport, navigate sensitive topics, and maintain participant confidentiality.
Communication Skills – Effective verbal and written communication skills with participants and internal study teams.
Team Collaboration – Ability to collaborate within multi‑disciplinary team settings and follow established workflows.
Flexibility – Availability to work evenings, overnight shifts, or weekends if required by study protocols.
Travel Readiness – Availability for local travel as necessary.
Other duties as assigned.
Job Responsibilities
Recruits, consents, screens, schedules, tracks, and provides study updates to participants throughout the conduct of the study.
Collects and enters data into study case report forms and/or electronic data capture system and responds to queries in a timely manner.
Assists in preparing simple data summaries, reports, or charts to support study documentation and reporting requirements.
Maintains accurate and complete procedural documentation including study participant and site‑level documentation in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.
Verifies data against 100% of source documentation for accuracy before entry into case report forms and electronic data capture systems to ensure timeliness and audit readiness.
May collect, process, and ship potentially biohazardous specimens.
Administers structured tests and questionnaires according to research study protocols; may utilize study‑related technology and equipment as part of assessment procedures.
Provides ongoing study status updates and responds to questions from PI, Administrator, department stakeholders, sponsor and compliance throughout the conduct of the study.
Maintains study flow by communicating promptly with study participants and coordinating with study team members as directed.
Participates in auditing and monitoring visits; gathers and communicates unanticipated problems (protocol deviations, adverse events, and serious adverse events).
Works with PI(s), sponsor, compliance, clinical staff and/or manager to identify and improve routine processes as it relates to the conduct of the research study.
Other duties as assigned.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
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Clinical Research Coordinator I-22430
at
Rush University Medical Center , Chicago, Illinois.
Job Summary The Clinical Research Coordinator I (CRC I) supports the conduct of clinical research studies across a range of disciplines. The CRC I receives direction from the principal investigator or supervisor and is responsible for participant recruitment and interaction, study data collection and entry, maintenance of study and regulatory documentation, sponsor communication, and adherence to study protocols and policies. The CRC I executes defined study tasks with guidance, ensuring operational compliance, accurate data entry, and participant safety.
Education Bachelor’s degree
Required Experience
0–2 years of experience in a research study or other relevant experience
OR, Two (2) years’ total experience, where 1 year is supporting or coordinating research studies
Preferred Experience Two (2) or more years prior experience in clinical research or related field
Knowledge, Skills, & Abilities
Time Management – Ability to meet deadlines and manage assigned study tasks.
Problem‑Solving – Ability to troubleshoot routine field issues and use discretion to elevate appropriately when unplanned events arise.
Attention to Detail – Strong attention to accuracy in data collection and documentation.
Participant Relations – Ability to build rapport, navigate sensitive topics, and maintain participant confidentiality.
Communication Skills – Effective verbal and written communication skills with participants and internal study teams.
Team Collaboration – Ability to collaborate within multi‑disciplinary team settings and follow established workflows.
Flexibility – Availability to work evenings, overnight shifts, or weekends if required by study protocols.
Travel Readiness – Availability for local travel as necessary.
Other duties as assigned.
Job Responsibilities
Recruits, consents, screens, schedules, tracks, and provides study updates to participants throughout the conduct of the study.
Collects and enters data into study case report forms and/or electronic data capture system and responds to queries in a timely manner.
Assists in preparing simple data summaries, reports, or charts to support study documentation and reporting requirements.
Maintains accurate and complete procedural documentation including study participant and site‑level documentation in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.
Verifies data against 100% of source documentation for accuracy before entry into case report forms and electronic data capture systems to ensure timeliness and audit readiness.
May collect, process, and ship potentially biohazardous specimens.
Administers structured tests and questionnaires according to research study protocols; may utilize study‑related technology and equipment as part of assessment procedures.
Provides ongoing study status updates and responds to questions from PI, Administrator, department stakeholders, sponsor and compliance throughout the conduct of the study.
Maintains study flow by communicating promptly with study participants and coordinating with study team members as directed.
Participates in auditing and monitoring visits; gathers and communicates unanticipated problems (protocol deviations, adverse events, and serious adverse events).
Works with PI(s), sponsor, compliance, clinical staff and/or manager to identify and improve routine processes as it relates to the conduct of the research study.
Other duties as assigned.
Rush is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.
#J-18808-Ljbffr