Clinical Research Assistant — Study Coordination & Data

DHR Health; Edinburg (TX); On-site; USD 36,000 - 48,000; Full time

Job summary

DHR Health Institute for Research and Development in Edinburg, TX is seeking a Clinical Research Assistant to support administrative and clinical tasks within the Research Department. Responsibilities include triaging participants, phlebotomy activities, data entry into CRFs/EDC, sample handling, and coordinating registrations for clinical trials.

The role emphasizes compliance with state and federal regulations, with duties spanning study preparation, participant support, data/documentation,

Qualifications

• High School diploma or GED required or preferred.
• CNA/MA/PCA or similar program preferred.
• BLS certification required.
• Microsoft Office proficiency required.
• Strong written and verbal communication skills required.
• Evening or weekend availability may be required.
• Comfort with medical/technical terminology.

Responsibilities

• Prepare study materials and visit worksheets.
• Assist with regulatory paperwork and supply management.
• Schedule participant visits and reminders; escort to labs.
• Enter data into CRFs/EDC; maintain logs and study documents.
• Perform clerical tasks and manage study supplies.
• Assist with monitoring visits and audits preparation.
• Support training logs and consent form version control.
• Coordinate communication between participants, coordinators, and staff.

Skills

BLS Certification

Microsoft Office

Medical terminology

Written and verbal communication

Flexibility for evenings/weekends

Education

High School diploma or GED

CNA program / Medical Assistant / PCA or similar

Tools

MS Office Suite

Job description

DHR Health Institute for Research and Development in Edinburg, TX is seeking a Clinical Research Assistant to support administrative and clinical tasks within the Research Department. Responsibilities include triaging participants, phlebotomy activities, data entry into CRFs/EDC, sample handling, and coordinating registrations for clinical trials.

The role emphasizes compliance with state and federal regulations, with duties spanning study preparation, participant support, data/documentation,