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Clinical Research Coordinator

Job in Indian Village, Jackson County, Missouri, USA
Listing for: Saint Luke's Health System
Full Time position
Listed on 2026-08-27
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 50000 - 68000 USD Yearly USD 50000.00 68000.00 YEAR
Job Description & How to Apply Below
Location: Indian Village

Job Description 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.

Why Saint Luke’s?

We believe in creating a collaborative environment, while looking for innovative ways to improve.

We offer competitive salaries and benefits packages to all eligible employees:

  • Medical health plans
  • Tuition reimbursement
  • Leave of Absence, PTO, and various Welfare plans
  • Retirement contributions
  • Employee Assistance Program
  • #LI-CM1
Job Requirements
  • Applicable

    Experience:

    Less than 1 year
  • Bachelor's Degree
Job Details

Full Time Day (United States of America)

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.

Find out more about what Saint Luke’s offers: http://(Use the "Apply for this Job" box below).-lukes

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.
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