Description
SHIFT: No Weekends
SCHEDULE: Full-time
Sarah Cannon is the research arm of HCAs global cancer enterprise. Focused on advancing therapies for patients, it is one of the worlds 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.
We believe our success is dependent on a healthy work environment where you are the core of advancing therapies and accelerating drug development. We apply the same compassion and commitment we have for our patients to our co-workers and colleagues and promote an entrepreneurial culture.
Benefits:Tuition Reimbursement/Assistance Programs
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 an Enrollment Research Nurse your primary responsibility is to screen and enroll oncology research study subjects ensuring protocol compliance. You will enroll patients onto clinical trials through recruitment, screening, enrollment and follow-up of eligible subjects.
- You will be familiar with the protocols on which the patients are enrolled, screen, treat.
- You will review the study design and inclusion/exclusion criteria with physician and patient.
- You will complete and document screening/eligibility and consent accurately and have all parties fully execute the document including HIPAA Authorization
- Complete the inclusion/exclusion form and standard enrollment form accurately and 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 screen every new patient or patient returning to office with scan results and document appropriately on the patient tracking logs
- You will complete the study medication order form and have the physician or nurse practitioner sign orders prior to treatment and ensure that all medications, including antiemetics, are approved by the registrar prior to initiating treatment or when changing medication regimens, such as crossover studies
- Accurately calculate and the BSA, creatinine clearance, urine protein:creatinine ratio or any other conversions needed per protocol
- You will obtain completed and signed waivers prior to submitting forms to enrollment coordinator for investigator-initiated protocols and re-consent patients in a timely manner and document process appropriately
Qualifications
What you should have for this role:
Associate of Nursing Degree; Bachelor of Nursing is preferred.
Nursing license for the State of Tennessee
Knowledge of medical and oncology research terminology and of federal regulations, good clinical practices (GCP).
One year of clinical nursing experience
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.
Notice
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