Clinical Research Assistant

Job overview

The Clinical Research Assistant role is onsite in Port Arthur, TX. Compensation is not specified. The assistant supports Iterative Health’s clinical research team and active clinical trials. Working under the Principal Investigator and site management, the assistant supports study activities from participant screening and enrollment through documentation, data entry, and compliance. The role helps research teams conduct trials accurately while protecting participant rights and maintaining study records.

What you'll do

• Assist with communicating study requirements
• support recruitment strategies in accordance with site policies and IRB requirements
• screen participants using protocol criteria
• register participants in the CTMS
• report recruitment and enrollment metrics
• maintain study documentation and files
• enter visit data in eCRF and CTMS
• store study documents securely
• maintain study supplies and accountability records when applicable
• process and ship specimens per protocol and IATA regulations as directed
• support daily study activities and communications
• assist with participant rights and compliance.

What we're looking for

Skills & competencies

clinical research assistant

port arthur tx

iterative health

full-time

clinical trials

participant screening

study documentation

ctms

ecrf

gcp

specimen processing

healthcare experience

Work arrangement

• Weekend coverage required

Why this role

Entry point into clinical research with exposure to the full study lifecycle; requires a high school diploma or equivalent and at least two years of healthcare-setting experience; some college coursework preferred.

About the employer

Iterative Health is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.