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WA
Clinical Research Coordinator II - Neurology
Washington University in St. Louis4488 Forest Park, United States, United Statesfull_timeVerifiedPosted 6 Feb 2025
💰 $78,900/yr($52,600/yr – $78,900/yr)
About the role
Scheduled Hours
40Position Summary
This position is looking for a Social Worker to assist Memory and Aging Project (MAP) Investigators as coordinator of a basic to moderately complex clinical research study while providing resources and support to our research participants and their families; may be responsible for multiple research studies simultaneously, acting as a liaison with the Investigator, school, community and the study participants; responsible for managing and recording all phases of study protocol as required by protocol guidelines.Job Description
Primary Duties & Responsibilities:
- Routinely 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 informed consent; explains study components/ as they relate to overall purpose of the research; uses critical thinking 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.
- Provides resources and education to MAP participants and their caregivers about dementia and dementia care.
- Prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
- Confers with PI to assist in developing plans for research projects and discuss the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate Coordinates the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding.
- Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events; Conducts Clinical Assessments of participants using structured clinical instruments with supervision from the PI.
- Performs other duties incidental to the work described herein.
Working Conditions:
Job Location/Working Conditions
Patient care setting.
Physical Effort
Typically sitting at desk or table.
Equipment
Office equipment.
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 must be obtained within one month of hire date.
- Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirement).
Preferred Qualifications
Education:
M.S.W. - Master of Social Work
Certifications:
Work Experience:
Skills:
Clinical Research, Clinical Study Protocols, Database Management, Interpersonal Communication, Microsoft Word, Organizing, Research Projects, Social Work, Spreadsheet Analysis, Statistical Analysis Software (SAS)Grade
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