Full employer posting
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
Monday - Friday, Days 8 am until 4:30 pm. Job Requirements Applicable
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
About the role
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).