Clinical Research Coordinator I — Kickstart Your Trial Career

Iterative Health; Port Arthur (TX); On-site; USD 48,000 - 72,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator I in Port Arthur, TX to support daily trial activities and patient visits. This role involves coordinating protocol tasks, patient recruitment, consent, and data entry within a dynamic clinical research environment.

The CRC will perform blood draws, vital signs, ECGs, and medication dispensing while ensuring trial compliance and regulatory standards. Open to relocation and collaboration with multidisciplinary teams across sites.

Qualifications

• Minimum 1–2 years of clinical research experience.
• Ability to execute study tasks with guidance from PIs and management.
• Strong written and verbal communication skills.

Responsibilities

• Administratively and clinically manage industry-sponsored trials.
• Lead patient recruitment activities and verify informed consent.
• Schedule patient visits and conduct visits per protocol.
• Perform blood draws, dispense medication, and record vitals/ECGs.

Skills

Patient recruitment

Phlebotomy

ECG

Data entry

Medical terminology

Team coordination

Education

Associate or Bachelor’s degree in clinical/science

Medical Assistant or LPN certification

Tools

CTMS

EDC

IATA regs

Job description

Iterative Health is seeking a Clinical Research Coordinator I in Port Arthur, TX to support daily trial activities and patient visits. This role involves coordinating protocol tasks, patient recruitment, consent, and data entry within a dynamic clinical research environment.

The CRC will perform blood draws, vital signs, ECGs, and medication dispensing while ensuring trial compliance and regulatory standards. Open to relocation and collaboration with multidisciplinary teams across sites.