Site Research Assistant - Kansas City, MO
$52,000–$81,120 year
On-siteKansas City, Missouri, United States
Job Summary
Perform EDC data entry, resolve queries, and review patient charts to support protocol-required workflows. Assist with prescreening referrals, recruiting, and enrolling study participants while managing visit scheduling and reminders. Collect participant history, coordinate laboratory requirements, and record vital signs as required by protocol. Support the informed consent process and maintain regulatory binders while ensuring compliance with GCP and IRB requirements. This part-time role (24 hours/week) is based in Kansas City, MO, and requires an associate's degree or equivalent with at least one year of clinical research experience.
Required Qualifications
- Minimum of an associate's degree or equivalent education and experience
- At least 1 year of experience in a clinical research setting
- Working knowledge of clinical trials, GCP, and study-specific procedures
- Ability to perform required clinical procedures and understand medical terminology
- High attention to detail with strong organizational and multitasking abilities
- Ability to collaborate effectively with coworkers, physicians, patients, and study stakeholders
- Certifications and licenses as required by local, state, or regulatory bodies
- Ability to support patient prescreening activities including chart review
- Ability to support data entry/query tasks
- Ability to support additional administrative tasks as needed
Desired Qualifications
- At least 1 year of experience in a clinical research setting (preferred)
- Familiarity with cardiovascular studies (preferred)
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