Clinical Research Coordinator

Department:
SOM KC Kidney Institute (KI)

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Jared Grantham Kidney Institute
Position Title:
Clinical Research Coordinator
Job Family Group:
Professional Staff
Job Description Summary:
Provide administrative and research support for clinical research projects by working with the Research Institute, other departments, and outside entities cooperating in research efforts. 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. Work with research teams for protocol management and to ensure compliance with protocols guidelines, institutional policies, and procedures, as well to strict adherence to the Good Clinical Practice Guideline. Interact with participants in clinical research studies. Identify problems and/or inconsistencies and monitor participants’ progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols
Job Description:
Under the direction of PI, recruit and educate patients for clinical trials and evaluate potential patient eligibility for clinical trials. Perform or schedule subject visit procedures, phlebotomy and sample collection, sample processing, handling, shipping as required by the protocol. Produce reports as requested by physician PIs and nurse coordinators. Assist Investigators and study team with preparation and analysis of study data for publication and grant preparation.Develops study-specific or program data acquisition forms in RedCap. Accurately enter data from various sources and files paper CRFs in study binders. Assist nurse coordinators with collating and maintaining clinical information from multiple sources into research charts, study binders, etc. Assist nurse coordinators with collating and maintaining clinical information from multiple sources into research charts, study binders, etc. Administratively supports the research nurses and PIs with study start-up activities, recruitment, preparing documents, paying bills, ordering supplies, updating the study log and maintaining electronic and paper based filing systems. Supports the goals and activities of the Kidney Institute and assists with actively promoting and increasing awareness of our clinical trial program, Other duties as assigned. ** Required Qualifications ** Bachelor’s degree in basic science, health related field, or management. Experience may substitute for a degree on a year to year basis. Must have 2 or more years’ experience in clinical research. Must have experience in phlebotomy and specimen processing. Excellent communication, writing, organizational, and presenting skills. Ability to interact with multidisciplinary teams including patients, families, physicians, and administrative staff. ** Preferred Qualifications ** Demonstrates knowledge of databases, spreadsheet, and word processing software. Certification by ACRP or SoCra as a clinical research coordinator. RN-BS degree in nursing with current Kansas RN Licensure..
Employee Type:
Regular
Time Type:
Full time
Pay Rate Type:
Salary
Pay Grade:
108
Pay Range:

Minimum

$53,000.00

Midpoint

$68,000.00

Maximum

$83,000.00