Clinical Research Coordinator

Saint Luke's Health System•Kansas City, MO

3d•Onsite

About The Position

Saint Luke’s Hospital in Kansas City, MO is seeking a Research Coordinator to join our research team to assist with providing and coordinating care for patients active in various research studies. As a Clinical Research Coordinator in this position, you will prepare the site for conduct of the study identify potential study participants, conduct informed consent, assist with scheduling labs and appointments, gather and record study related data, and provide patient education for various research studies. Shift Details: Monday – Friday This is a wonderful opportunity to work with nationally recognized providers and leaders in Cancer research and treatment options. We are seeking an experienced Research Coordinator. This team is innovative and is working with cutting edge technologies and procedures while evolving medicine in oncology care. We are seeking an organized, flexible, adaptable coordinator that can manage various tasks, projects, and deadlines simultaneously. 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. Saint Luke’s Health System includes 18 hospitals and campuses across the Kansas City region, home care and hospice, behavioral health care, dozens of physician practices, a life care senior living community, and more.

Requirements

Bachelor's degree is required
Applicable Experience: Less than 1 year

Responsibilities

Supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Works under the direction of the clinical Principal Investigator (PI).
Works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.
Prepare the site for conduct of the study identify potential study participants
Conduct informed consent
Assist with scheduling labs and appointments
Gather and record study related data
Provide patient education for various research studies.