Job Description​

The Clinical Research Nurse has multiple responsibilities related to clinical research studies. These responsibilities may vary according to study protocol. The primary activities include, but are not limited to:

• Assisting in the evaluation of new protocols for feasibility at the site

• Preparing the site for conduct of the study such as establishing study files and training study related staff

• Disseminating study information to physicians and ancillary departments

• Preparing the Institutional Review Board submissions performing informed consent process with potential subjects coordinating study conduct throughout the trial screening and recruiting subjects gathering and recording study related data according to protocol

• Overseeing drug device accountability maintaining regular communications with sponsors or CROs and IRBs

• Collaborating with other SLH departments providing study services.

This position requires RN license in MO & KS.

Job Requirements

Applicable Experience:

2 years

Cert Clinical Research Coordinator - 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)

Bachelor's Degree

Job Details

Full Time

Day (United States of America)

The best place to get care. The best place to give care. Saint Luke’s 12,000 employees strive toward that vision every day. Our employees are proud to work for the only faith-based, nonprofit, locally owned health system in Kansas City. Joining Saint Luke’s means joining a team of exceptional professionals who strive for excellence in patient care. Do the best work of your career within a highly diverse and inclusive workspace where all voices matter.

Join the Kansas City region's premiere provider of health services. Equal Opportunity Employer.