Oncology Research Nurse — Clinical Trials Lead

Ironwood Women's Centers

Phoenix (AZ)

On-site

USD 70,000 - 90,000

Full time

6 days ago
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Benefits offered by this job

Health/dental/vision
Life insurance
401K
Competitive salary

Job summary

Ironwood Cancer & Research Centers in Surprise, AZ, is seeking a dynamic Research Nurse to coordinate oncology clinical trials across our Phoenix-area locations. The role is full-time, Monday through Friday, with no on-call or weekend requirements.

You will oversee protocol adherence, consent, data entry, regulatory filings, and collaboration with investigators. Travel between offices is expected, and a strong background in clinical research and nursing is essential.

Qualifications

  • Oncology/clinical research experience required.
  • Nursing degree from accredited program; B.S.N. preferred.
  • GCP/training in human subjects desirable.
  • CCRC certification preferred.
  • Must be willing to travel between offices.

Responsibilities

  • Review studies for feasibility with investigators and director.
  • Screen, consent, enroll subjects and supervise non-RN coordinators.
  • Maintain data and regulatory files; adverse event reporting.
  • Ensure proper billing for research subjects.
  • Prepare study submissions to IRB with regulatory docs.
  • Follow randomization and blinding procedures per protocol.
  • Ensure eligible patients consent appropriately and are enrolled.
  • Enter data accurately into sponsor databases and resolve queries.
  • Manage investigational product storage, accountability and dispensing.

Skills

Clinical skills
Organization
Leadership
Communication
Travel willingness

Education

Bachelor of Nursing
GCP training
IATA training
CCRC certification

Tools

Microsoft Office

Job description

Ironwood Cancer & Research Centers in Surprise, AZ, is seeking a dynamic Research Nurse to coordinate oncology clinical trials across our Phoenix-area locations. The role is full-time, Monday through Friday, with no on-call or weekend requirements.

You will oversee protocol adherence, consent, data entry, regulatory filings, and collaboration with investigators. Travel between offices is expected, and a strong background in clinical research and nursing is essential.

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