Clinical Research Coordinator I – Psychiatry
Company | Wash U |
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Location | Lake St Louis, MO, USA |
Salary | $47400 – $71200 |
Type | Full-Time |
Degrees | Bachelor’s, Master’s |
Experience Level | Entry Level/New Grad, Junior |
Requirements
- Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).
- No specific work experience is required for this position.
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.
- Collects clinical data under clinical research protocols.
- Experience working in a mental health setting such as a clinic, psychiatric hospital, or crisis response center.
- Strong understanding of mental health disorders.
- Performs other duties as assigned.
Preferred Qualifications
- Master’s degree – Psychology
- Conducting Cognitive Or Clinical Assessments With Children And/Or Adults With Psychiatric Disorders (1 Year)
- Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Crisis Response, Interpersonal Communication, Mental Health, Organizing, Physician Communications, Research Support, Working with Children