Clinical Research Coordinator I: Driving Patient-Centric Trials

Iterative Health; Beaumont (TX); On-site; USD 52,000 - 76,000; Full time

Job summary

Iterative Health, a healthcare technology and services company, is seeking a full-time Clinical Research Coordinator (CRC) in Beaumont, TX. The CRC will support daily trial activities and coordinate patient visits, maintain study documentation, and ensure compliance with GCP and FDA guidelines.

Relocation is open. Ideal candidates have 1–2 years of clinical research experience, strong communication skills, and a background in clinical or scientific fields.

Qualifications

• 1–2 years of clinical research experience preferred.
• Experience executing study tasks with guidance from PIs and management.
• Ability to read and apply clinic policies and research protocols.
• Strong written and verbal communication skills.

Responsibilities

• Administer and coordinate industry-sponsored clinical trials.
• Lead patient recruitment activities and verify informed consent.
• Schedule patient visits and procedures per protocol requirements.
• Conduct patient visits and collect vital signs; perform ECGs.

Skills

Clinical research coordination

Patient recruitment

CTMS familiarity

Effective communication

Education

Associate or Bachelor’s in clinical/scientific field

Tools

CTMS

Microsoft Office

Job description

Iterative Health, a healthcare technology and services company, is seeking a full-time Clinical Research Coordinator (CRC) in Beaumont, TX. The CRC will support daily trial activities and coordinate patient visits, maintain study documentation, and ensure compliance with GCP and FDA guidelines.

Relocation is open. Ideal candidates have 1–2 years of clinical research experience, strong communication skills, and a background in clinical or scientific fields.