Détails du poste

As an Enrollment Research Nurse your primary responsibility is to screen and enroll oncology research study subjects ensuring protocol compliance.You willenroll 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, treated.  

• 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 

• You will 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  and 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  

​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 

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S. Please click here to learn more about our research offerings.

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.