Oncology Clinical Research Coordinator (Day Shift)

bannerhealth

Gilbert (AZ)

On-site

USD 60,000 - 80,000

Full time

14 days+
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Job summary

Banner Health in Gilbert, Arizona, is seeking a Clinical Research Coordinator to coordinate and implement protocols, collect medical data, and support patient assessments within the Gateway Oncology research program. The role includes recruiting participants, maintaining study files, and communicating with the study team and sponsors.

The candidate will assist in adverse event triage, provide patient education, and ensure accurate documentation and regulatory compliance for ongoing clinical

Qualifications

  • Knowledge of clinical research methodologies typically obtained with a bachelor's degree in a healthcare field.
  • Strong organizational and task management abilities.
  • Excellent communication skills and ability to maintain confidentiality of patient and study information.
  • Familiarity with federal and state regulations governing clinical practice and research policies.

Responsibilities

  • Coordinate and implement assigned protocols and collect/record medical data.
  • Assist in patient assessments, recruit/screen volunteers, and manage study files.
  • Triages adverse events and communicates with the research physician regarding events.
  • Provide educational information to patients and families and act as a liaison within the clinical research program.
  • Prepare IRB forms, informed consents, and sponsor communications in a timely manner.

Skills

Clinical research methodologies
Organization
Communication skills
Confidentiality

Education

Bachelor's degree in a healthcare field

Job description

Banner Health in Gilbert, Arizona, is seeking a Clinical Research Coordinator to coordinate and implement protocols, collect medical data, and support patient assessments within the Gateway Oncology research program. The role includes recruiting participants, maintaining study files, and communicating with the study team and sponsors.

The candidate will assist in adverse event triage, provide patient education, and ensure accurate documentation and regulatory compliance for ongoing clinical

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