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WA
Clinical Research Coordinator I - Psychiatry
Washington University in St. Louis4444 Forest Park Ave., United States, United Statesfull_timeVerifiedPosted 1 Aug 2025
💰 $71,200/yr($47,400/yr – $71,200/yr)
About the role
Scheduled Hours
40Position Summary
We are seeking a Clinical Research Coordinator with experience in human subject research to help coordinate a multi-disciplinary study. The principal investigators for the study are from the Departments of Psychiatry and Psychological Brain Sciences. Full-time effort will be dedicated to this project. We are seeking an individual with experience working with pregnant women, parents and/or young children and diverse populations. This is a complex and large interdisciplinary study, and this individual should have experience with this type of research.Job Description
Primary Duties & Responsibilities:
- Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
- Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
- Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient’s timely completion of protocol requirements; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
- Provide guidance and develop workflow for staff to help accomplish the study aims, semi-structured parent interviews, behavioral assessments in young children, biospecimen collection, and neuroimaging.
- Collects clinical data under clinical research protocols.
- Performs other duties as assigned.
Required Qualifications
Education:
Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
Certifications:
Work Experience:
Skills:
Driver's License:
More About This Job
Required Qualifications:
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).
Preferred Qualifications
Education:
No additional education beyond what is stated in the Required Qualifications section.
Certifications:
Work Experience:
Skills:
Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Interpersonal Communication, Neuroimaging, Organizing, Research Support, Teamwork, Working with ChildrenGrade
C09Salary Range
$47,400.00 - $71,200.00 / AnnuallyThe salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications aApply for this role
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