Clinical Research Nurse 1 - Oncology-30452
Rush University Medical Center · Chicago, Illinois, United States
Full-time
Posted Oct 14, 2026
Job Description
Location: Chicago, Illinois
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Cancer Center-Res Fac
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (8:00:00 AM - 5:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $40.75 - $64.89 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
Summary
The Clinical Research Nurse 1 (CRN 1) is a licensed nurse who delivers clinical care to research participants while supporting the conduct of clinical studies under the direction of a Principal Investigator (PI). Working as part of a multidisciplinary research team, this role assists with participant recruitment, eligibility screening, informed consent, and protocol adherence.
The CRN 1 monitors participants for changes in health status, manages adverse event reporting, and administers study medications when applicable. The nurse educates physicians and staff on study procedures and keeps the clinical team informed about protocol updates and participant status changes.
This entry-level research nursing role requires strong foundational nursing skills, a willingness to learn clinical research regulations, and the ability to communicate with diverse participants and care teams. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Required Job Qualifications
Education: Bachelor of Science in Nursing (BSN) OR Master of Science in Nursing (MSN)
Experience: Two years of clinical nursing practice experience required
Licenses: Current State of Illinois Registered Nurse Licensure
Certifications: Current Basic Life Support certification for Healthcare Professionals
Knowledge, Skills, And Abilities
Regulatory Compliance Awareness – Able to demonstrate introductory knowledge of Good Clinical Practices and/or Good Documentation Practices, human subjects protections, institutional, local, state and federal guidelines and regulations related to clinical research
Communication Skills – Ability to communicate complex clinical and regulatory concepts in easy-to-understand language.
Participant Engagement – Ability to build rapport with diverse participants and peers
Judgment & Escalation – Demonstrated problem-solving, critical decision making, and professional judgment Time Management – Strong organizational skills and attention to detail
Teamwork & Collaboration – Ability to work successfully both independently and in team settings.
Flexibility – Flexible work hours and travel may be required
Preferred Job Qualifications
Experience: Two years of experience in clinical research as appropriate to study population.
Certifications: Clinical specialty certification appropriate to study population
Job Responsibilities
Relationships and Caring
Delivers protocol-required nursing care to research participants, including monitoring of health status and documentation
Follows participant care plans based on protocol requirements and participant needs
Assesses participant status and communicates follow-up needs to the PI or interdisciplinary care team in alignment with protocol
Communicates study details and updates to participants, families, and interdisciplinary care team members
Educates interdisciplinary care teams on protocol requirements
Notifies the PI and care team of changes in participant health status.
Evidence-Based Practice
Performs protocol-defined procedures including medication administration, clinical assessments, and sample collection under supervision.
Ensure accurate documentation of tasks performed
Schedules study visits and prepares materials and source documentation per protocol.
Reminds participants of required tests or procedures
Reviews and enters data into study systems accurately and on time
Coordinates specimen handling and shipping; ensures compliance with sponsor and federal safety requirements
Recognizes and reports unexpected events, documentation errors, or potential deviations to appropriate staff.
Reports protocol deviations and serious adverse events to the study sponsor and IRB as applicable
Systems Use and Documentation
Maintains current knowledge of disease-specific conditions and research trends relevant to assigned studies.
Completes all required protocol-specific and system trainings
Applies ALCOA principles to ensure high-quality documentation and data entry across systems
Navigates multiple systems (including OnCore, REDCap, Epic) to manage participant data, schedule visits and support workflow accuracy
Critical Thinking
Reviews patient charts and study eligibility criteria; seeks additional information to ensure accurate enrollment, if needed.
Supports recruitment activities for assigned study participants
Tracks visit schedules and confirms that study procedures, labs, and documentation are completed per protocol.
Identifies and communicates potential issues or protocol deviations to the PI or manager
Maintains routine communication with PI and study team regarding visit completion and participant status, including changes in health status
Prepares basic documentation and supports monitoring and audit readiness under supervision
Provides required visit data and procedural documentation in CTMS or other systems to support financial tracking and billing accuracy
Leadership
Participates in study team meetings and follows assigned responsibilities to support clinical research activities.
Assists in orienting new research staff to study procedures under supervision
Assists in preparing regulatory documents and collaborates with regulatory coordinators to submit IRB forms or updates, as directed
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.
Business Unit: Rush Medical Center
Hospital: Rush University Medical Center
Department: Cancer Center-Res Fac
Work Type: Full Time (Total FTE between 0.9 and 1.0)
Shift: Shift 1
Work Schedule: 8 Hr (8:00:00 AM - 5:00:00 PM)
Rush offers exceptional rewards and benefits learn more at our Rush benefits page (https://www.rush.edu/rush-careers/employee-benefits).
Pay Range: $40.75 - $64.89 per hour
Rush salaries are determined by many factors including, but not limited to, education, job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush’s anticipated wage or salary reasonably expected to be offered for the position. Offers may vary depending on the circumstances of each case.
Summary
The Clinical Research Nurse 1 (CRN 1) is a licensed nurse who delivers clinical care to research participants while supporting the conduct of clinical studies under the direction of a Principal Investigator (PI). Working as part of a multidisciplinary research team, this role assists with participant recruitment, eligibility screening, informed consent, and protocol adherence.
The CRN 1 monitors participants for changes in health status, manages adverse event reporting, and administers study medications when applicable. The nurse educates physicians and staff on study procedures and keeps the clinical team informed about protocol updates and participant status changes.
This entry-level research nursing role requires strong foundational nursing skills, a willingness to learn clinical research regulations, and the ability to communicate with diverse participants and care teams. Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.
Required Job Qualifications
Education: Bachelor of Science in Nursing (BSN) OR Master of Science in Nursing (MSN)
Experience: Two years of clinical nursing practice experience required
Licenses: Current State of Illinois Registered Nurse Licensure
Certifications: Current Basic Life Support certification for Healthcare Professionals
Knowledge, Skills, And Abilities
Regulatory Compliance Awareness – Able to demonstrate introductory knowledge of Good Clinical Practices and/or Good Documentation Practices, human subjects protections, institutional, local, state and federal guidelines and regulations related to clinical research
Communication Skills – Ability to communicate complex clinical and regulatory concepts in easy-to-understand language.
Participant Engagement – Ability to build rapport with diverse participants and peers
Judgment & Escalation – Demonstrated problem-solving, critical decision making, and professional judgment Time Management – Strong organizational skills and attention to detail
Teamwork & Collaboration – Ability to work successfully both independently and in team settings.
Flexibility – Flexible work hours and travel may be required
Preferred Job Qualifications
Experience: Two years of experience in clinical research as appropriate to study population.
Certifications: Clinical specialty certification appropriate to study population
Job Responsibilities
Relationships and Caring
Delivers protocol-required nursing care to research participants, including monitoring of health status and documentation
Follows participant care plans based on protocol requirements and participant needs
Assesses participant status and communicates follow-up needs to the PI or interdisciplinary care team in alignment with protocol
Communicates study details and updates to participants, families, and interdisciplinary care team members
Educates interdisciplinary care teams on protocol requirements
Notifies the PI and care team of changes in participant health status.
Evidence-Based Practice
Performs protocol-defined procedures including medication administration, clinical assessments, and sample collection under supervision.
Ensure accurate documentation of tasks performed
Schedules study visits and prepares materials and source documentation per protocol.
Reminds participants of required tests or procedures
Reviews and enters data into study systems accurately and on time
Coordinates specimen handling and shipping; ensures compliance with sponsor and federal safety requirements
Recognizes and reports unexpected events, documentation errors, or potential deviations to appropriate staff.
Reports protocol deviations and serious adverse events to the study sponsor and IRB as applicable
Systems Use and Documentation
Maintains current knowledge of disease-specific conditions and research trends relevant to assigned studies.
Completes all required protocol-specific and system trainings
Applies ALCOA principles to ensure high-quality documentation and data entry across systems
Navigates multiple systems (including OnCore, REDCap, Epic) to manage participant data, schedule visits and support workflow accuracy
Critical Thinking
Reviews patient charts and study eligibility criteria; seeks additional information to ensure accurate enrollment, if needed.
Supports recruitment activities for assigned study participants
Tracks visit schedules and confirms that study procedures, labs, and documentation are completed per protocol.
Identifies and communicates potential issues or protocol deviations to the PI or manager
Maintains routine communication with PI and study team regarding visit completion and participant status, including changes in health status
Prepares basic documentation and supports monitoring and audit readiness under supervision
Provides required visit data and procedural documentation in CTMS or other systems to support financial tracking and billing accuracy
Leadership
Participates in study team meetings and follows assigned responsibilities to support clinical research activities.
Assists in orienting new research staff to study procedures under supervision
Assists in preparing regulatory documents and collaborates with regulatory coordinators to submit IRB forms or updates, as directed
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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