Clinical Research Nurse - Oncology

saintlukes; Kansas City (MO); On-site; USD 75,000 - 95,000; Full time

Job summary

Saint Luke's Hospital in Kansas City, MO is seeking a Clinical Research Nurse to support oncology studies. The role includes coordinating daily study activities, conducting informed consent, and serving as the primary liaison among participants, investigators, sponsors, and CROs.

Ideal candidates will have 2 years of experience, an RN license valid in KS/MO, and an Associate Degree. This is a full-time on-site position with standard daytime hours.

Qualifications

• 2 years of applicable experience
• RN license KS/MO (NURSYS)
• Associate Degree required

Responsibilities

• Responsible for clinical operations activities for assigned studies & participants
• Single contact for participants, investigators, staff, sponsors and CROs
• Data entry and data query resolution in study databases
• Supports and coordinates daily clinical study activities
• Supports PI, department, sponsor and CRO inquiries
• Prepares and maintains research records per regulatory requirements
• Conducts informed consent
• Conducts screening and recruitment procedures

Skills

Data entry

Informed consent

Screening and recruitment

Data query resolution

Study coordination

Regulatory compliance

Education

Associate Degree

Registered Nurse license (KS/MO)

Job description

Job Description

Saint Luke's Hospital in Kansas City, Mo has an opportunity for a Clinical Research Nurse.

The Oncology 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.

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

The Schedule:

Monday - Friday, Days 8 am until 4:30 pm.

Job Requirements

Applicable Experience:

2 years

Registered Nurse (KS) Multi-State - 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)