Sarah Cannon Research Institute (SCRI) is looking to advance oncology treatments and improve outcomes for cancer patients by enrolling subjects onto clinical trials, requiring efficient and compliant screening and enrollment processes.
Requirements
- 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
Responsibilities
- Screen and enroll oncology research study subjects ensuring protocol compliance.
- Enroll patients onto clinical trials through recruitment, screening, enrollment and follow-up of eligible subjects.
- Review the study design and inclusion/exclusion criteria with physician and patient.
- 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.
- 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.).
- Accurately calculate and the BSA, creatinine clearance, urine protein:creatinine ratio or any other conversions needed per protocol.
Other
- Associate of Nursing Degree; Bachelor of Nursing is preferred.
- Nursing license for the State of Tennessee
- Mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
