Clinical Research Study Assistant I - Neurology
Quick Summary
Participant Recruitment, Screening, and Consent: Assists with the recruitment and screening of potential study participants in accordance with study protocols.
Participant Recruitment, Screening, and Consent: Assists with the recruitment and screening of potential study participants in accordance with study protocols.
Responsibilities
~2 min readParticipant Recruitment, Screening, and Consent:
- →Assists with the recruitment and screening of potential study participants in accordance with study protocols.
- →Reviews medical records and other relevant information to assess preliminary eligibility for participation.
- →Explains study procedures and requirements to participants and their caregivers or legally authorized representatives, as applicable.
- →Obtains informed consent in accordance with approved protocols and institutional requirements.
Study Visit Coordination and Participant Support:
- →Schedules study visits and follow-up appointments and coordinates required study procedures.
- →Prepares study packets, questionnaires, and other materials needed for participant visits.
- →Assists with study visits by escorting participants to designated areas and coordinating their movement through various visit procedures.
- →Explains and coordinates laboratory testing, diagnostic procedures and other study-related activities.
- →Provides participants and caregivers with study-related information and directs them to appropriate resources as needed.
Data Collection and Documentation:
- →
Collects and records research data from participant interviews, questionnaires, medical records, diagnostic tests, and other approved sources. - →Completes study forms, source documentation, and other required paperwork in accordance with study protocols and regulatory requirements.
- →Performs basic, protocol-defined assessments and assists with the review of collected data for completeness and accuracy.
- →Prepares and maintains study documentation and reports as required.
Laboratory and Clinical Research Support:
- →Assists with the collection, processing, labeling, storage and preparation of blood and other biological specimens for research purposes, as trained and authorized.
- →Coordinates laboratory testing and other diagnostic procedures required by study protocols.
- →Maintains study supplies an ensures that necessary materials are available for participant visits and research activities.
General Research Support:
- →Works collaboratively with Research Coordinators, PIs and other research team members to support study activities.
- →Performs other duties as assigned to support the successful conduct of clinical research studies.
Job Location/Working Conditions:
- Normal office environment
Physical Effort:
- Typically sitting at a desk or table
Equipment:
- Office equipment
Requirements
~1 min readAbout 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
About this job
- Pay per year
- ≈ $37,211–$54,808 a year
- 32% below the $68,076 median for Other jobs on Jobera (131,167 salaries).
- Posted
- 7 days ago
Listing Details
- Posted
- October 23, 2026
- First seen
- October 26, 2026
- Last seen
- October 30, 2026
Posting Health
- Days active
- 4
- Repost count
- 0
- Trust Level
- 40%
- Scored at
- October 30, 2026
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