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Clinical Research Coordinator (2)

Job Description
Superlanet is seeking a Clinical Research Coordinator to join our healthcare client's oncology research team in Arizona. This is a direct hire, onsite role supporting innovative clinical trials and driving excellence in patient care and research execution.

The Clinical Research Coordinator (RN) is responsible for overseeing and managing the daily operations of oncology clinical research trials. Working directly with Principal Investigators (PIs), this role ensures compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. The RN acts as a liaison between patients, providers, sponsors, and institutional stakeholders, while also performing patient assessments and delivering comprehensive research coordination.

Key Responsibilities:

  • Collaborate with investigators to determine study eligibility and ensure proper documentation per protocol.
  • Educate patients and families about clinical trials, consent processes, and study expectations.
  • Coordinate study activities including scheduling, data collection, and follow-ups for oncology trials.
  • Monitor patient adherence and manage adverse events in collaboration with care teams.
  • Ensure accurate and timely documentation within the electronic medical record and study files.
  • Participate in study site visits, audits, and sponsor communications.
  • Maintain strict compliance with all federal, state, and institutional regulations regarding human subject protection.
  • Lead patient visits, administer protocol-required assessments, and track investigational product usage.
  • Provide education and training to nursing staff and research teams on trial protocols and best practices.
  • Maintain secure and organized study records, including source documents and regulatory files.

Qualifications:

  • Education: Graduate from an accredited nursing program (BSN preferred).
  • Experience: Minimum of 3 years of nursing experience, with oncology experience strongly preferred.
  • Licensure/Certifications:

    • Current Registered Nurse (RN) license valid in the state of Arizona.
    • Current BLS or ACLS certification

Knowledge, Skills & Abilities:

  • Strong understanding of nursing care, oncology practices, and clinical assessments.
  • Working knowledge of clinical research protocols, human subject protections, and federal regulations.
  • Excellent communication skills; able to explain complex clinical information in a patient-friendly manner.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint), Adobe, and Teams/SharePoint.
  • Experience with clinical documentation systems and research data entry tools.



Benefits

Salary based on experience

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Clinical Research Coordinator (2)

Superlanet
Tucson, AZ
Full Time
Certification

Published on 10/19/2025

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