Clinical Research Coordinator

2 weeks ago

Kansas City, United States Medix™ Full time

Clinical Research Coordinator - Kansas City, MO


Hours: Monday - Friday, 8am-5pm

Pay: $25 - $30/hour

Location: Kansas City, Missouri 64151


We are seeking an experienced Clinical Research Coordinator to join one of America's largest rheumatology clinics and research facilities.


Responsibilities:

  • Enroll patients into clinical research studies following established protocols and procedures.
  • Obtain informed consent from study participants, ensuring they understand the purpose, procedures, risks, and benefits of the study.
  • Coordinate and conduct patient visits according to the study schedule.
  • Monitor and document patient progress and report any adverse events or protocol deviations to the principal investigator.
  • Actively recruit potential study participants by foPerform venipuncture to collect blood samples for clinical research and diagnostic purposes, ensuring patient comfort and adherence to protocol.
  • Perform venipuncture to collect blood samples for clinical research and diagnostic purposes, ensuring patient comfort and adherence to protocol.
  • Conduct and process laboratory tests, ensuring accurate and timely collection of specimens for research studies.
  • Administer electrocardiograms (EKGs) to monitor and record participants' cardiac activity as required by study protocols.
  • Administer medications, both oral and injectable, to study participants according to prescribed protocols and safety guidelines.
  • Collaborate with nursing staff to assist with the preparation and administration of intravenous infusions, ensuring proper technique and participant safety.
  • Maintain controlled environmental conditions for study supplies and medications, ensuring adherence to specified temperature and storage requirements.
  • Manage inventory of study-related materials, including tracking, ordering, and replenishing supplies as needed to support ongoing research activities.


Qualifications:

  • 2 years experience as a CRC
  • Strong patient facing and a patient recruitment background


Preferred Qualifications:

  • Background in Oncology or Rheumatology
  • Bachelors degree
  • ACRP or SOCRA certified
  • Phase II-III pharma experience

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