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Clinical Research Coordinator / Registered Nurse

The University of Kansas Health System St. Francis Campus
Posted a month ago, valid for 18 days
Location

Topeka, KS, US

Salary

Competitive

Contract type

Full Time

Paid Time Off
Tuition Reimbursement

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Sonic Summary

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  • Join our team as a full-time Clinical Research Coordinator Registered Nurse in Topeka, Kansas, working day shifts.
  • Candidates must be a Registered Nurse with a minimum of 2 years of clinical research experience and a Bachelor's degree.
  • The position involves collaborating with multidisciplinary teams to manage clinical research studies and monitor participant progress.
  • The organization offers a people-first environment with career growth opportunities, comprehensive health benefits, and paid time off.
  • Salary details are not specified, but the role emphasizes a supportive culture and advanced technology to enhance patient care.
Overview

Join our team as a day shift, full-time, Clinical Research Coordinator Registered Nurse in Topeka, Kansas.  Must be an Registered Nurse.

 

Why Join Us?

 

Thrive in a People-First Environment and Make Healthcare Better

  • Thrive: We empower our team with career growth opportunities, tuition assistance, and resources that support your wellness, education, and financial well-being.
  • People-First: We prioritize your well-being with paid time off, comprehensive health benefits, and a supportive, inclusive culture where you are valued and cared for.
  • Make Healthcare Better: We use advanced technology to support our team and enhance patient care.

Get to Know Your Team:

  • The University of Kansas Health System St. Francis Campus, a part of a rich legacy of compassionate care since 1909, now offers 378 licensed beds, a history of innovation, and strong community support.

Responsibilities

  • This position is responsible for working collaboratively with multidisciplinary teams, research and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research.
  • The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data.
  • Monitor participants’ progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols.

Qualifications

Job Requirements:

  • Must be an RN
  • 2 Years of Clinical Research experience and a Bachelors degree required.



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