Clinical Research Coordinator II: Trials Lead & Patient Care

Iterative Scopes

Beaumont (TX)

On-site

USD 70,000 - 90,000

Full time

14 days+

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Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily trial activities and ensure protocol compliance. You will drive patient enrollment, manage visit schedules, and maintain study documentation across complex studies.

With a focus on high-quality execution, you’ll collaborate with investigators, sponsors, CROs, and internal teams while upholding GCP, HIPAA, and regulatory standards.

Qualifications

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

Responsibilities

  • Coordinate industry-sponsored trials from start-up through closeout with minimal supervision.
  • Manage complex visit schedules and protocol activities to meet timelines.
  • Lead patient recruitment, outreach, and enrollment tracking to support goals.
  • Conduct protocol visits and appropriate procedures per GCP and site SOPs.
  • Maintain study documentation, data entry, and timely data queries.
  • Prepare for sponsor/CRO/regulatory visits and audits.

Skills

Clinical trial coordination
GCP compliance
Patient recruitment
Documentation & data entry
Sponsor/CRO communications

Education

Associate’s or Bachelor’s degree in a scientific/healthcare field

Tools

CTMS
EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily trial activities and ensure protocol compliance. You will drive patient enrollment, manage visit schedules, and maintain study documentation across complex studies.

With a focus on high-quality execution, you’ll collaborate with investigators, sponsors, CROs, and internal teams while upholding GCP, HIPAA, and regulatory standards.

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