Oncology Research Nurse: Lead Trials & Patient Care

Regional One Health

Memphis (TN)

On-site

USD 80,000 - 110,000

Full time

5 days ago
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Job summary

Regional One Health is seeking an Oncology Research Nurse Coordinator to lead multiple complex oncology trials within the ROHRI. The role focuses on promoting research, accelerating processes, and driving patient accrual in a supportive hospital-based research institute.

The coordinator will collaborate with sponsors, investigators, and clinical teams to ensure protocol compliance, safety, and timely study execution across trial lifecycles.

Qualifications

  • Associate's Degree in Nursing is required.
  • Bachelor's Degree in Nursing is a plus.
  • Registered Nurse licensure in TN is required.
  • Research certification is a plus but not required.
  • Minimum 1 year experience in Oncology and Clinical Research is required.
  • At least 1 year experience in Oncology as an RN; 3+ years preferred.
  • At least 1 year experience in subjects enrollment in clinical trials; 3+ years preferred.

Responsibilities

  • Work closely with sponsor for expectations and timelines throughout trial life cycle.
  • Collaborate with investigators and clinical team to ensure trial compliance and progress.
  • Perform and/or coordinate all research procedures applicable to the position.
  • Perform nursing procedures related to research, ensuring subject safety and protocol compliance.
  • Partner with research team to achieve goals and cohesive operations.

Education

Associate's Degree in Nursing
Bachelor's Degree in Nursing
Registered Nurse licensure in TN
Research certification (preferred)
Oncology/Clinical Research experience (1+ years)

Job description

Regional One Health is seeking an Oncology Research Nurse Coordinator to lead multiple complex oncology trials within the ROHRI. The role focuses on promoting research, accelerating processes, and driving patient accrual in a supportive hospital-based research institute.

The coordinator will collaborate with sponsors, investigators, and clinical teams to ensure protocol compliance, safety, and timely study execution across trial lifecycles.

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