Independent Clinical Research Coordinator II

Iterative Health

Amarillo (TX)

Sur place

USD 65 000 - 90 000

Plein temps

Il y a 3 jours
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Résumé du poste

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure adherence to protocol requirements, regulatory standards, and patient safety guidelines. You will manage complex studies with minimal oversight while partnering with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution.

The role emphasizes patient recruitment, protocol compliance, and collaboration across multiple stakeholders

Qualifications

  • 3–5 years of clinical research or healthcare experience.
  • Bachelor’s degree in a scientific, healthcare, or related discipline required.
  • Experience in gastroenterology, hepatology, or cardiology is preferred.

Responsabilités

  • Coordinate industry-sponsored clinical trials from start-up through closeout with minimal supervision.
  • Lead patient recruitment and enrollment tracking to support study goals.
  • Conduct protocol-required patient visits and assessments per GCP and site SOPs.
  • Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections.
  • Maintain accurate study documentation and ensure timely data entry and queries resolution.
  • Provide ongoing communication with sponsors, CROs, investigators, and internal teams.

Connaissances

Clinical research experience
Regulatory knowledge
Study coordination
Patient recruitment

Formation

Bachelor’s degree in science/healthcare

Outils

CTMS
EDC systems
Office software

Description du poste

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure adherence to protocol requirements, regulatory standards, and patient safety guidelines. You will manage complex studies with minimal oversight while partnering with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution.

The role emphasizes patient recruitment, protocol compliance, and collaboration across multiple stakeholders

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