Clinical Research Coordinator II - Impactful Trials

Iterative-Health

Beaumont (TX)

On-site

USD 52,000 - 78,000

Full time

14 days+
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Job summary

Iterative Health in Beaumont, TX is seeking a Clinical Research Coordinator II to independently coordinate daily trial activities and ensure protocol, regulatory, and patient safety compliance. This role partners with investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success.

The CRC II will manage complex studies with minimal supervision, focusing on patient visits, data integrity, and site operations to support GI, hepatology, obesity, and

Qualifications

  • Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
  • 3-5 years of clinical research or healthcare experience.
  • Experience in gastroenterology, hepatology, or cardiology preferred.
  • CCRC® or CCRP® certification preferred or equivalent.
  • Proficiency with CTMS, EDC systems, and standard office software.

Responsibilities

  • Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout.
  • Manage complex study visit schedules and protocol-related activities to meet timelines.
  • Lead patient recruitment and retention, including chart review, outreach, informed consent, and enrollment tracking.
  • Conduct protocol-required patient visits and assessments per GCP, SOPs, and study protocol.

Skills

Clinical research experience
Healthcare experience
Study coordination

Education

Associate’s or Bachelor’s degree in science/healthcare

Tools

CTMS
EDC systems

Job description

Iterative Health in Beaumont, TX is seeking a Clinical Research Coordinator II to independently coordinate daily trial activities and ensure protocol, regulatory, and patient safety compliance. This role partners with investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success.

The CRC II will manage complex studies with minimal supervision, focusing on patient visits, data integrity, and site operations to support GI, hepatology, obesity, and

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