Bilingual Clinical Trials Research Assistant

Johnson County Clin Trials (JCCT); Houston (TX); On-site; USD 34,000 - 42,000; Full time

Job summary

Johnson County Clin Trials (JCCT) seeks a Research Assistant to support clinical operations and study teams in executing trial activities. You will assist with document prep, data entry, subject recruitment, and protocol-specific tasks in a regulated environment.

Reporting to the Site Manager or Director, you will collaborate with Clinical Research Coordinators to ensure compliance with GCP/SOPs, maintain source documents, and contribute to high-quality trial conduct across multiple studies at

Qualifications

• High school diploma or GED required.
• Bachelor's degree preferred.
• Experience in clinical research setting or related environment preferred.
• Certification as a Medical Assistant preferred.
• At least one year of experience in medical history, medication history, and vital signs preferred.
• Familiarity with clinical trial management systems is a plus.

Responsibilities

• Ensure confidentiality of clinical research volunteers and sponsors.
• Maintain high level of customer service within the department.
• Assist in maintenance of Clinical Conductor.
• Maintain ERP system: preparing, filing, updates and archiving study information.
• Perform data entry and query resolution.
• Prepare, handle, distribute, track and maintain trial supplies.
• Assist with pre-screening, screening, recruitment and enrollment.

Skills

Communication skills

Bilingual Spanish/English

Organizational skills

Attention to detail

MS Office

Medical terminology

Independent worker

Problem solving

EDC familiarity

Project coordination

Education

High school diploma or GED

Bachelor's degree

Clinical research experience

Medical Assistant certification

Tools

Medidata Rave

Inform

TrialKit

Job description

Johnson County Clin Trials (JCCT) seeks a Research Assistant to support clinical operations and study teams in executing trial activities. You will assist with document prep, data entry, subject recruitment, and protocol-specific tasks in a regulated environment.

Reporting to the Site Manager or Director, you will collaborate with Clinical Research Coordinators to ensure compliance with GCP/SOPs, maintain source documents, and contribute to high-quality trial conduct across multiple studies at