Clinical Research Coordinator II - Biomedical Engineering
Quick Summary
Human Subjects Research Identify eligible volunteers with SCI from participant databases Screen and recruit participants across study protocols Coordinate scheduling among participants, study staff,
Bachelor’s degree or combination of education and/or experience may substitute for minimum education. Certifications/Professional Licenses:The list below may include all acceptable certifications,
This is a hands-on, participant-facing position that combines two functions: (1) clinical research coordination across multiple funded clinical trials, including recruitment, scheduling, and regulatory compliance; and (2) direct support of experimental sessions with participants with SCI, including participant preparation, transfers and positioning, and familiarity with research instrumentation.
The position is well suited to candidates with a background in physical therapy, athletic training, exercise or movement science, or a related health or life science field who want substantive research training, co-authorship opportunities, and sustained contact with the SCI community. Recent graduates are encouraged to apply.
Responsibilities
~1 min readHuman Subjects Research
- →Identify eligible volunteers with SCI from participant databases
- →Screen and recruit participants across study protocols
- →Coordinate scheduling among participants, study staff, and clinical evaluators
- →Serve as the primary point of contact for study participants; arrange transportation and process payments
- →Maintain scheduling calendars, visit tracking logs, and participant communication records
Experimental Session Support (hands-on)
- →Assist in preparing participants for testing sessions, including skin preparation, electrode placement, transfers, and positioning
- →Monitor participant comfort and safety; document session notes and flag adverse events or protocol deviations
- →Maintain experimental supplies and ensure post-session equipment cleanup
Regulatory Oversight and Compliance
- →Prepare and submit IRB applications, amendments, and continuing reviews
- →Maintain ClinicalTrials.gov registration and reporting
- →Keep study binders, delegation logs, enrollment records, and source documents in audit-ready condition
- →Track and coordinate study staff training and certifications (CITI, GCP, BLS)
Perform other duties as assigned.
Requirements
~1 min readBasic 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).
About the Role
~1 min readFor frequently asked questions about the application process, please refer to our External Applicant FAQ.
If you are unable to use our online application system and would like an accommodation, please email CandidateQuestions@wustl.edu or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.
All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.What We Offer
~1 min readPersonal
Location & Eligibility
Listing Details
- First seen
- October 11, 2026
- Last seen
- October 11, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 51%
- Scored at
- October 11, 2026
Signal breakdown
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