Sarah Cannon Research Institute (SCRI) is looking to advance oncology treatments and improve outcomes for cancer patients by screening and enrolling patients in oncology research studies.
Requirements
- Proficiency in HIPAA compliance, Good Clinical Practice (GCP), and FDA regulations
- In-depth understanding of clinical research methodologies
- One year of clinical nursing experience
- One year of clinical research experience is preferred
- One year of experience treating oncology patients is preferred
Responsibilities
- Facilitates patient enrollment in clinical trials by conducting recruitment, screening, enrollment, and follow-up activities in accordance with protocol requirements.
- Reviews the medical records of prospective study participants to confirm eligibility as defined by the protocol.
- Documents and evaluates medical history, concomitant medications, prior therapies, and adverse events.
- Utilizes the study protocol as the primary reference for patient screening.
- Informs and educates patients throughout the enrollment process, including screening and treatment steps.
- Reviews study design and inclusion/exclusion criteria with both physician and patient.
- Verifies that all medications are approved by the protocol before starting treatment or when adjusting medication regimens, such as during crossover studies.
Other
- Associate of Nursing Degree; Bachelor of Nursing is preferred.
- Nursing license for the State of Texas
- Desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.
- Applications will be accepted through October 9, 2025.
