Oncology Research Nurse Coordinator in Orlando, Florida, United States
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UCF Lake Nona Medical Center

Oncology Research Nurse Coordinator

Orlando, FL, United States
Full-time • Days 7-10 Hrs/Wkdays Only
Job ID: 4771
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Description

Sarah Cannon is the research arm of HCA’s global cancer enterprise. Focused on advancing therapies for patients, it is one of the world’s leading clinical research organizations conducting community-based clinical trials in oncology, cardiology and orthopedics through affiliations with a network of more than 1,000 physicians across the United States and United Kingdom.

You contribute to our success. Every role has an impact on our patients’ lives and you have the opportunity to make a difference. We are looking for a dedicated Oncology Research Nurse like you to be a part of our team!

At Sarah Cannon, we want to ensure your needs are met. We offer a variety of comprehensive medical, dental, and vision plans along with some unique benefits including:

  • Tuition Reimbursement/Assistance Programs|
  • Student Loan Repayment
  • Paid Personal Leave
  • 401k (100% annual match – 3%-9% of pay based on years of service)
  • Identity Theft Protection discounts
  • Auto, Home, and Life Insurance options
  • Adoption Assistance
  • Employee Stock Purchase Program (ESPP)

As the Oncology Research Nurse your primary responsibility is to screen, enroll and follow oncology research study subjects ensuring protocol compliance and close monitoring while the subjects are on study.

  • You are responsible for all data collection, source documentation and submission of adverse experience reports.
  • You will support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.
  • You will use the protocol as the only tool to screen, treat, and follow patients
  • You will assess the patient and document findings at each clinic visit while on protocol
  • You will document all specific tools required by the protocol (i.e. oral medication forms, pill count diaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws, etc.)
  • You will document any interaction regarding the patient that occurs while the patient is enrolled on a protocol, including follow-up and survival (this includes home health intervention, pharmacies, study managers, physicians, and clinic colleagues)

Qualifications

What you should have for this role:

  • An Associate of Nursing Degree; Bachelor of Nursing is preferred.
  • Knowledge of medical and oncology research terminology and of federal regulations, good clinical practices (GCP). 
  • One year of clinical research experience is preferred
  • One year of experience treating oncology patients is preferred

Do you want to be a part of a team working together to fight cancer? We are so excited to speak with you about this phenomenal opportunity. Apply to hear more.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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Details

Full-time • Days 7-10 Hrs/Wkdays Only

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