Clinical Research Intern — AI-Driven Trials & Recruitment

Iterative Health; Cedar Park (TX); On-site; USD 36,000 - 48,000; Full time

Job summary

Iterative Health in Cedar Park, Texas, is seeking a full-time, on-site Research Intern to support Clinical Research Coordinators in daily trial activities. You will help assess patient eligibility, screen potential participants, and manage recruitment networks within protocol and IRB requirements.

You will document patient data in the CTMS, assist with recruitment strategies, and learn to navigate EMR and study protocols under supervision.

Qualifications

• Strong written and verbal communication skills.
• Ability to read, interpret, and apply clinic policies and research protocols.
• Ability to use standard office software.
• Must be able to lift up to 25 pounds.

Responsibilities

• Assist clinical research staff with reviewing protocols for patient eligibility criteria
• Assist with managing recruitment and referral networks, screening subjects for eligibility using inclusion/exclusion criteria
• Learn to navigate EMR and other clinical databases
• Document patient information in the Clinical Trials Management System
• Develop and implement recruitment strategies in line with IRB approvals
• Under guidance, navigate study protocols and chart reviews to complete tasks
• Protect the rights and welfare of human research participants per regulations
• Cooperate with site compliance and PHI access/disclosure controls
• Other duties as assigned

Skills

Strong written and verbal comms

Policy/protocol interpretation

Office software proficiency

Lifts up to 25 pounds

Education

High school diploma or equivalent

Some college preferred

Job description

Iterative Health in Cedar Park, Texas, is seeking a full-time, on-site Research Intern to support Clinical Research Coordinators in daily trial activities. You will help assess patient eligibility, screen potential participants, and manage recruitment networks within protocol and IRB requirements.

You will document patient data in the CTMS, assist with recruitment strategies, and learn to navigate EMR and study protocols under supervision.