Clinical Research Nurse - Oncology

Saint Luke's Health System

Kansas City, MOOn-siteFull time
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Location
Kansas City, MO
Work style
On-site
Job type
Full time
Posted
Oct 15
5 days ago
Career path

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About the company

Saint Luke's Health System

Hospital & health care · 10,001+ employees

Saint Luke's Health System on LinkedIn

What you'll do

  • Coordinates clinical study activities and supports study participants, investigators, sponsors, and staff.
  • Manages study data and records, conducts informed consent, and carries out screening and recruitment procedures.

What you need

  • Requires 2 years of applicable experience, an associate degree, and Registered Nurse licensure in Kansas and Missouri.
  • Education: an associate degree

Key skills

Registered Nurse (KS) Multi-StateRegistered Nurse (MO)

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Read the full posting here
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)

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