Neurology Clinical Research Assistant II – MS Trials

Washington University in St. Louis; Missouri; On-site; USD 28,000 - 41,000; Full time

Job summary

Washington University in St. Louis invites applications for a Clinical Research Study Assistant II in Neurology.

This on-campus role supports a team of coordinators and a research nurse to screen, consent, and enroll participants in industry-sponsored trials focused on MS and related neurological conditions. Responsibilities include data extraction, paperwork, scheduling visits, and ensuring protocol compliance.

Qualifications

• High school diploma or equivalent.
• Basic Life Support certification must be obtained within one month of hire date.
• Administrative or research experience (2 years).
• Strong ability to communicate effectively with individuals.
• Detail-oriented approach to tasks.
• Informed consent discussions with patients in clinical trials.

Responsibilities

• Assists clinical research coordinators with management of clinical trials: screening, enrolling, preparing informed consent packets, extracting data from source documents and reporting in data entry systems.
• Completes paperwork/documentation according to study protocol.
• Interviews study subjects and schedules follow-ups.
• Performs basic/scripted assessments to confirm eligibility.
• Explains and schedules laboratory and diagnostic procedures as required.
• Collects data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; prepares reports.
• Assists with study sample tracking and shipping.
• Performs other duties as assigned.

Skills

Clinical Trials

Data Collection Methods

Detail-Oriented

Diagnostic Testing

Interpersonal Communication

Oral Communications

Organizing

Screenings

Written Communication

Education

High School Diploma or Equivalent

Associate Degree

Job description

Washington University in St. Louis invites applications for a Clinical Research Study Assistant II in Neurology.

This on-campus role supports a team of coordinators and a research nurse to screen, consent, and enroll participants in industry-sponsored trials focused on MS and related neurological conditions. Responsibilities include data extraction, paperwork, scheduling visits, and ensuring protocol compliance.