University of Kansas Medical Center·Kansas City, Missouri
The Clinical Research Assistant supports clinical trials through participant recruitment, data collection, and maintaining regulatory compliance. They coordinate study logistics, manage documentation, and serve as a primary point of contact for study participants.
SOM KC Internal Medicine - Pulmonary, Critical Care, and Sleep Medicine
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Clinical Research Assistant - Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine)
Job Description: SUMMARY:
The Clinical Research Assistant (CRA) in the Division of Pulmonary, Critical Care, and Sleep Medicine supports clinical trials by assisting with various aspects of research, including participant recruitment, data collection, and compliance with regulatory guidelines. They work under the guidance of principal investigators and research coordinators to ensure the smooth and efficient execution of studies.
Assist Clinical Research Coordinators (CRCs) with study setup, participant recruitment efforts, and follow-ups.
Prepare and organize research study materials, including participant packets, consent forms, and regulatory documentation.
Schedule study-related appointments and coordinate participant visits.
Maintain an up-to-date inventory of study supplies and assist in ordering necessary materials.
Serve as a point of contact for study participants, providing general study information and answering non-clinical questions.
Assist with scheduling and sending reminders for study visits.
Provide participants with instructions regarding study expectations, visit logistics, and follow-up care.
Escort study participants to different departments or areas for required study procedures.
Collect, enter, and maintain research data in electronic and paper-based systems.
Ensure proper documentation and organization of study records, regulatory binders, and case report forms.
Assist with maintaining compliance with institutional and regulatory guidelines by supporting the CRC in IRB submissions and protocol updates.
Assist in preparing materials for audits, sponsor site visits, and regulatory inspections.
Track and report study milestones and participant recruitment status.
Maintain study logs and ensure proper filing of all study-related correspondence.
Support the CRC in coordinating study team meetings, taking meeting minutes, and preparing reports.
This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice.
Two (2) years’ experience in health sciences, biology, nursing, or a related field. Education may be substituted for experience on a year for year basis.
Education: Bachelor’s degree in health sciences, biology, nursing, or a related field
Time type: Full time
The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above.
$22.88 - $33.17
$22.88
$28.03
$33.17
Requires two years of experience in health sciences, biology, nursing, or a related field, which may be substituted by education. A bachelor's degree and experience with REDCap, Epic, and IRB regulations are preferred.
Market context
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