Bilingual Clinical Research Assistant

Johnson County Clintrials LLC; Houston (TX); On-site; USD 38,000 - 56,000; Full time

Job summary

JCCT is seeking a Research Assistant to support clinical trial operations within the Clinical Operations department. The role involves administrative and operational tasks, including data entry, document preparation, and subject recruitment, under the guidance of Study Coordinators.

The position emphasizes compliance with study protocols, GCP, and SOPs, while maintaining confidentiality and high-quality standards.

Qualifications

• High school diploma or GED required.
• Bachelor’s degree preferred.
• Experience in clinical research setting 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

• Support study coordinators and the study team in executing clinical trial activities.
• Provide administrative and operational support for trials, including document preparation and data entry.
• Maintain confidentiality and ensure compliance with GCP and SOPs.
• Assist with pre-screening, screening, recruitment and enrollment of subjects.
• Record vital signs and collect specimens per protocol.
• Track and manage study-related documents and supplies.

Skills

Excellent communication

Bilingual Spanish-English

Organizational skills

Detail oriented

MS Office proficiency

Medical terminology knowledge

Team collaboration

Problem solving

Project management basics

Education

High school diploma or GED

Bachelor’s degree (preferred)

Medical Assistant certification (preferred)

Tools

Medidata Rave

Inform

TrialKit

Microsoft Office Suite

Job description

JCCT is seeking a Research Assistant to support clinical trial operations within the Clinical Operations department. The role involves administrative and operational tasks, including data entry, document preparation, and subject recruitment, under the guidance of Study Coordinators.

The position emphasizes compliance with study protocols, GCP, and SOPs, while maintaining confidentiality and high-quality standards.