Independent Clinical Research Coordinator II

TAU Ventures

Lubbock (TX)

On-site

USD 65,000 - 90,000

Full time

6 days ago
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Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials from start-up through closeout, ensuring protocol compliance and patient safety. The role requires managing complex visit schedules and leading recruitment efforts to support enrollment goals.

You will perform protocol-required visits and procedures, maintain study documentation, and collaborate with sponsors, CROs, investigators, and site teams to drive high-quality

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® or equivalent certification preferred.

Responsibilities

  • Coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision.
  • Manage complex study visit schedules and protocol-related activities to meet timelines.
  • Lead patient recruitment and retention activities including chart review, outreach, informed consent discussions, and enrollment tracking.
  • Conduct protocol-required patient visits and assessments per GCP and SOPs.
  • Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections.

Skills

Organizational skills
Prioritization
Communication skills

Education

Associate’s or Bachelor’s degree

Tools

CTMS
EDC systems

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate industry-sponsored clinical trials from start-up through closeout, ensuring protocol compliance and patient safety. The role requires managing complex visit schedules and leading recruitment efforts to support enrollment goals.

You will perform protocol-required visits and procedures, maintain study documentation, and collaborate with sponsors, CROs, investigators, and site teams to drive high-quality

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