Clinical Research Coordinator II - Biomedical Engineering

About this role

Location ST. LOUIS, MO 63130

 Scheduled Hours 37.5

Position Summary The Seáñez Lab in the Department of Biomedical Engineering studies how neuroprosthetics and motor training can improve movement in people with spinal cord injury (SCI). We are seeking a Clinical Research Coordinator II to serve as the operational center of our human subjects research program.

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.

Job Description

Primary Duties & Responsibilities:

Human 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.

Working Conditions: Job Location/Working Conditions • Patient care setting.  

Physical Effort • Typically sitting at desk or table.  

Equipment • Office equipment.

The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.

Required Qualifications

Education: 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, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.

Basic Life Support - American Heart Association, Basic Life Support - American Red Cross Work Experience: Clinical Research (2 Years) Skills: Not Applicable Driver's License: A driver's license is not required for this position.

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: No additional education unless stated elsewhere in the job posting. Certifications /Professional Licenses : No additional certification/professional licenses unless stated elsewhere in the job posting. Work Experience: No additional work experience unless stated elsewhere in the job posting.

Skills: Clinical Research, Clinical Study Protocols, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)

Grade C10

Salary Range $54,600.00 - $81,900.00 / Annually

The 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 and performance, equity with others in the department, market rates for positions within the same grade and department budget.

Questions For frequently asked questions about the application process, please refer to our External Applicant FAQ .

Accommodation 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.

Pre-Employment Screening All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening.

Benefits Statement Personal • Up to 22 days of vacation, 10 recognized holidays, and sick time.

• Competitive health insurance packages with priority appointments and lower copays/coinsurance.

• Take advantage of our free Metro transi

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