Clinical Research Coordinator

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Center for Clinical Research Staff
Position Title:
Clinical Research Coordinator
Job Family Group:
Professional Staff
Job Description Summary:
The Clinical Research Coordinator will conduct participant visits, data entry, regulatory files, and the coordination of multiple psychiatry clinical studies. The Clinical Research Coordinator will work under a Research Manager, and with multiple principal investigators, who will assign all work to the research coordinator, who will work independently to complete assigned tasks with review by the supervisor. The research coordinator will collaborate with university partners (other departments within the KU School of Medicine, and other external partners) to accomplish project goals. This position will carry the on-call phone after hours as assigned. Light travel may be required.
This position will pay between $19.80 – $22.08 per hour commensurate with experience.
Job Description:

Required Qualifications:

• Bachelor’s degree in a health/science related field or a combination of education and equivalent experience

• Experience with Microsoft Office

• Experience with data entry

Preferred Qualifications:

• Training or experience in the medical field.

• Advanced training or experience in research methods and analysis

• Experience with clinical trials with human subjects

• Familiarity with Institutional Review Board (IRB) regulations pertaining to human subjects

• Experience with entering medical  data into online case report forms

• Ability to be self-directed, manage, organize, set and accomplish project goals

• Excellent writing skills

• Effective communication skills

• Ability to establish priorities, procedures, and methods working independently

• Ability to multi-task

• Detail oriented

Job Duties Outlined:

• Collect, manage, analyze, and report data related to assigned project activities

• Prepare Institutional Review Board proposals and related paperwork

• Maintain communication with project partners on research study activity

• Coordinate with Principal Investigator and study participants to schedule participant visits

• Interact directly with study participants during study visits

• Assist with site initiation visits and site monitoring visits

• Attend start up training/Investigator Meeting for new studies as required

• Liaison with sponsor contact

• Assist with study recruitment activities

This position 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.

Required Documents:

• Resume/CV

• Cover Letter

Employee Type:
Regular
Time Type:
Full time
Rate Type:
Hourly
Pay Range:
$19.80 – $28.70

Minimum

$19.80

Midpoint

$24.25

Maximum

$28.70