Clinical Research Study Assistant — Coordinating Trials

UNKNOWN; Northaven (MO); On-site; USD 27,000 - 41,000; Full time

Job summary

Washington University in St. Louis is seeking a clinical research support professional to assist with participant screening, consent, and enrollment in studies. The role includes coordinating visits, collecting data, and preparing study documentation.

The position supports under supervision and involves working in a normal office environment with associated administrative tasks and compliance requirements.

Qualifications

• Education: High school diploma or equivalent.
• Certifications: Basic Life Support (BLS) from American Heart Association or American Red Cross.
• Work Experience: Administrative or Research (2 Years).
• Driver's License: Not required.

Responsibilities

• Participates in recruitment of study participants and screens for eligibility with informed consent.
• Completes paperwork and schedules follow-ups per protocol.
• Performs basic assessments and coordinates laboratory/diagnostic procedures.
• Collects data from participants and records, prepares reports and packets.

Skills

Interpersonal Communication

Oral Communications

Organizing

Written Communication

Education

High school diploma

Associate degree

Job description

Washington University in St. Louis is seeking a clinical research support professional to assist with participant screening, consent, and enrollment in studies. The role includes coordinating visits, collecting data, and preparing study documentation.

The position supports under supervision and involves working in a normal office environment with associated administrative tasks and compliance requirements.