Clinical Research Nurse: Study Coordinator & Participant Advocate

Saint Luke's; Kansas City (MO); On-site; USD 70,000 - 100,000; Full time

Job summary

Saint Luke's is seeking a Clinical Research Nurse to support daily study activities under the Principal Investigator. You will coordinate with investigators, sponsor, and CROs, conduct informed consent, and oversee data entry and regulatory files to ensure compliant study conduct.

The role emphasizes entry-level supervision with a focus on learning and professional growth, with full-time daytime hours, in the Kansas City area.

Qualifications

• 2 years of applicable experience in clinical research nursing or related field.
• CRP or equivalent certification preferred; RN licensure in KS/MO required.
• Knowledge of consent processes, regulatory requirements, and data management.

Responsibilities

• Perform standard nursing duties while coordinating daily clinical study activities.
• Serve as the primary contact for participants, investigators, and study staff.
• Ensure regulatory compliance, document management, and proper investigational product accountability.
• Conduct informed consent and assist with screening and recruitment procedures.

Skills

Clinical research

Nursing

Informed consent

Data entry

Recruitment procedures

Education

Associate Degree

RN KS licensure

RN MO licensure

Clinical Research Certification

Job description

Saint Luke's is seeking a Clinical Research Nurse to support daily study activities under the Principal Investigator. You will coordinate with investigators, sponsor, and CROs, conduct informed consent, and oversee data entry and regulatory files to ensure compliant study conduct.

The role emphasizes entry-level supervision with a focus on learning and professional growth, with full-time daytime hours, in the Kansas City area.