Clinical Research Nurse

Integrated Resources, Inc ( IRI ); Chicago (IL); On-site; USD 90,000 - 130,000; Full time

Job summary

Integrated Resources, Inc ( IRI ) is seeking a Clinical Research Nurse to support complex clinical trials under Principal Investigator and Research Manager direction. The role involves direct patient care, study documentation, regulatory compliance, and collaboration with investigators and sponsors.

Responsibilities include coordinating trials, conducting assessments, phlebotomy, data review, and ensuring adherence to GCP and SOPs.

Qualifications

• BSN completed and currently licensed as an Illinois RN.
• Experience in clinical trials or research coordination preferred.
• Ability to read and implement study protocols.
• Strong organizational and communication skills.
• Ability to perform phlebotomy as needed.

Responsibilities

• Coordinate and participate in clinical research trials conducted by the Institute for Population and Precision Health.
• Assist in planning and implementing clinical study goals, objectives, and patient enrollment strategies.
• Conduct participant assessments, including physical assessments, vital signs, and the collection of histories.
• Perform phlebotomy and other clinical research procedures as required.
• Maintain study records, track progress, and perform quality assurance activities.
• Compile, review, and analyze clinical research data for accuracy.
• Coordinate with medical staff, departments, and satellite facilities.
• Maintain knowledge of SOPs and GCP guidelines.
• Ensure activities comply with protocols and regulations.
• Provide guidance on protocol requirements and research practices.
• Maintain regulatory documentation and support IRB/FDA submissions.
• Prepare for audits and inspections.
• Contribute to improving clinical research practices and accountability.
• Apply critical thinking to evaluate problems and solutions.
• Perform other related duties as assigned.

Skills

Clinical research coordination

Regulatory compliance

Phlebotomy

GCP knowledge

Communication skills

Documentation & record-keeping

Education

BSN (Bachelor of Science in Nursing)

Tools

Epic EMR

Microsoft Word

Microsoft Excel

Adobe Acrobat

Job description

Typical Hours: 8:00 AM-2:00 PM or 8:00 AM-4:00 PM. The schedule can be discussed during the interview.

Required License: Current, valid Illinois Registered Nurse (RN) license

License Verification: The RN license must be verified.

Job Description:

• Under the direction of the Principal Investigator (PI), Co-Investigators, and Research Manager (RM), the Clinical Research Nurse supports the daily operations of complex clinical trials and helps ensure compliance with federal, institutional, and study-specific requirements.
• This role involves coordinating clinical research activities, providing direct patient care, maintaining study documentation, supporting regulatory compliance, and collaborating with investigators, sponsors, and institutional departments.
• The Clinical Research Nurse also serves as a clinical resource, helping improve research practices and supporting the administrative, financial, personnel, and compliance aspects of clinical studies.

Key Responsibilities:

• Coordinate and participate in clinical research trials conducted by the Institute for Population and Precision Health.
• Assist in planning and implementing clinical study goals, objectives, and patient enrollment strategies.
• Conduct participant assessments, including physical assessments, vital signs, and the collection of medical, surgical, social, and behavioral histories.
• Perform phlebotomy and other clinical research procedures as required.
• Develop and implement study procedures, maintain accurate study records, track study progress, and perform quality assurance activities.
• Compile, review, and analyze clinical research data to ensure accuracy and completeness.
• Coordinate with medical staff, university departments, ancillary departments, and satellite facilities.
• Maintain current knowledge of study protocols, internal standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
• Ensure clinical research activities comply with study protocols and applicable federal and institutional regulations.
• Provide investigators and research personnel with guidance on protocol requirements and clinical research practices.
• Maintain regulatory documentation and assist with submissions and reports to the Institutional Review Board (IRB), Food and Drug Administration (FDA), and Data and Safety Review Committee.
• Prepare for and assist with audits, inspections, and monitoring visits conducted by sponsors or regulatory agencies.
• Serve as a clinical resource and contribute to improving clinical research practices, quality, and accountability across the department.
• Apply critical thinking and sound judgment to evaluate problems and identify appropriate solutions.
• Perform other related duties as assigned.

Required Qualifications:

• Bachelor of Science in Nursing (BSN).
• Current, valid Registered Nurse (RN) license issued by the State of Illinois.
• Ability to use basic computer applications and learn new software as needed.
• Strong interpersonal, verbal, and written communication skills.
• Strong organizational skills, attention to detail, and the ability to prioritize multiple assignments.
• Ability to read, understand, and implement clinical trial protocols.
• Knowledge of patient care fundamentals, including aseptic principles and techniques.
• Ability to provide direct patient care in a professional and respectful manner.
• Fundamental knowledge of clinical research and Good Clinical Practice (GCP).
• Ability to read and interpret medical documents and clinical instruments.

Preferred Qualifications:

• Previous clinical research experience.
• Experience with phlebotomy and intravenous (IV) line placement.
• Experience using Epic or other electronic medical record (EMR) systems.
• Working knowledge of Microsoft Word, Excel, and Adobe Acrobat.
• Experience participating in protocol reviews and clinical trial evaluations.
• Strong data management and quality assurance skills.

Work Environment and Additional Requirements:

• Work is performed in an office and clinical setting.
• Occasional evening or weekend hours may be required for enrollment events at community partner locations.
• Travel may be required to support enrollment events at community partner locations.