Site Research Assistant - McAllen, TX
$52,000–$81,120 year
On-siteMcAllen, Texas, United States
Job Summary
Perform EDC data entry and query resolution while reviewing patient charts from site databases to support protocol tasks. Assist with participant screening, prescreening referrals, and enrollment, managing scheduling and follow-up care coordination. Collect participant history, coordinate laboratory requirements, and record vital signs as required by the study protocol. Support the informed consent process and maintain study supplies and regulatory binders in strict adherence to GCP, IRB, and company SOPs. This Spanish bilingual role requires at least one year of clinical research experience and is scheduled for 24 hours per week on-site in McAllen, TX.
Required Qualifications
- Minimum of an associate's degree or equivalent combination of education and experience
- At least 1 year of experience in a clinical research setting
- Working knowledge of clinical trials, GCP principles, and study-specific procedures
- Familiarity with cardiovascular studies
- Demonstrated experience with reviewing charts from site databases
- Demonstrated experience with prescreening referrals
- Demonstrated experience with EDC entry and query resolution
- Demonstrated experience with visit scheduling and reminders
- Demonstrated experience with maintaining study supplies
- Demonstrated experience with upkeep of regulatory binders
- Demonstrated experience with recording (not obtaining) vital signs
- Ability to perform required clinical procedures and understand medical terminology
- High attention to detail and strong organizational skills
- Ability to collaborate effectively with coworkers, physicians, patients, and study stakeholders
- Certifications and licenses as required by company, state, country, or regulatory bodies
- Spanish Bilingual
Desired Qualifications
- At least 1 year of experience in a clinical research setting (preferred)
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