Clinical Research Assistant: Study Coordination

Iterative Health; Mansfield, Northern (TX, KY); Hybrid; USD 36,000 - 54,000; Full time

Job summary

Iterative Health is seeking a detail‑oriented Research Assistant to support day‑to‑day clinical trial activities on site in Mansfield, TX. You will assist with participant screening, enrollment, data entry, and documentation under the PI and study team.

The role emphasizes compliance with GCP, accurate data capture in CTMS/eCRF, and collaboration across study teams. Prior healthcare experience and strong communication are required for success.

Qualifications

• High school diploma or equivalent required; some college coursework preferred.
• Minimum 2 years of experience in a healthcare setting.
• Strong written and verbal communication skills.
• Ability to read, interpret, and apply clinic policies and research protocols.
• Familiarity with CTMS or eCRF platforms a plus.

Responsibilities

• Assist the Study Team with communicating study requirements to all individuals involved in the study.
• Work with the Study Team to develop and implement recruitment strategies in accordance with site policies and IRB requirements.
• Assist with screening subjects for eligibility using protocol inclusion/exclusion criteria.
• Register participants in the CTMS to ensure proper billing of study procedures.
• Enter patient visit data in eCRF and CTMS daily or as directed.
• Arrange secure storage of study documents in accordance with GCP guidelines.
• Maintain inventory of study supplies and investigational material accountability.
• Process and ship specimens per study protocol and IATA regulations.

Skills

Communication

Documentation

Team‑oriented

Detail‑oriented

Time management

Education

High school diploma

Some college coursework preferred

Tools

CTMS

eCRF

Job description

Iterative Health is seeking a detail‑oriented Research Assistant to support day‑to‑day clinical trial activities on site in Mansfield, TX. You will assist with participant screening, enrollment, data entry, and documentation under the PI and study team.

The role emphasizes compliance with GCP, accurate data capture in CTMS/eCRF, and collaboration across study teams. Prior healthcare experience and strong communication are required for success.