Clinical Research Nurse - RN

Saint Luke's; Kansas City (MO); Sur place; USD 70 000 - 100 000; Plein temps

Résumé du poste

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.

Responsabilités

• 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.

Connaissances

Clinical research

Nursing

Informed consent

Data entry

Recruitment procedures

Formation

Associate Degree

RN KS licensure

RN MO licensure

Clinical Research Certification

Description du poste

Job Description

The Clinical Research Nurse, in addition to performing standard nursing duties, plays a critical role in the conduct of clinical studies by supporting, facilitating, and coordinating the daily clinical study activities under the direction of the Principal Investigator (PI). The Clinical Research Nurse works with the PI, department, sponsor, and institution to support and provide guidance on the administration, compliance, financial, required personnel and other aspects of clinical studies . The Clinical Research Nurse oversees investigational drug and/or device accountability.

Job Description

The Clinical Research Nurse, in addition to performing standard nursing duties, plays a critical role in the conduct of clinical studies by supporting, facilitating, and coordinating the daily clinical study activities under the direction of the Principal Investigator (PI). The Clinical Research Nurse works with the PI, department, sponsor, and institution to support and provide guidance on the administration, compliance, financial, required personnel and other aspects of clinical studies . The Clinical Research Nurse oversees investigational drug and/or device accountability.

FT- Days, no weekends or holidays

• Requires a higher level of supervision by Lead/Manager, with expectation of continuous progress in learning/understanding of role.
• Responsible for clinical operations activities for assigned studies & participants
• Serves as single contact person for research participants, Investigators, clinic and ancillary staff, Sponsors, and CROs
• Responsible for data entry, data query resolution in clinical study database, as well as other study-specific system management for assigned studies
• Supports, facilitates, and coordinates daily clinical study activities in support of study conduct
• Supports PI, departmental, Sponsor, and CRO inquiries
• Prepares/maintains research records and files in concert with regulatory requirements and Institutional files
• Conducts informed consent
• Conducts screening and recruitment procedures

Job Requirements

Applicable Experience:
2 years

Cert Clinical Research Professional - Academy of Clinical Research Professionals, Registered Nurse (KS) - National Council of State Boards of Nursing (NURSYS), Registered Nurse (MO) - National Council of State Boards of Nursing (NURSYS)

Associate Degree

Job Details

Full Time

Day (United States of America)