Sarah Cannon Research Institute
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Overview
As an Oncology Research Nurse at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will screen, enroll and follow oncology research study subjects, ensuring protocol compliance and close monitoring while patients are on the study. You are responsible for data collection, source documentation, and submission of adverse event reports. Responsibilities
You will support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects. You will ensure the protection of study patients by timely adherence to protocol requirements and compliance. You will attend weekly study status teleconferences and monthly staff meetings. You will be familiar with the protocols on which the patients are enrolled, screen, treat, and follow patients. 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 (e.g., oral medication forms, pill count diaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws). 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; ensure medications, including antiemetics, are approved by the registrar prior to initiating treatment or when changing regimens (e.g., crossover studies). You will calculate the BSA, creatinine clearance, urine protein:creatinine ratio or other conversions 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 the process appropriately. You will accurately complete and submit follow-up serious adverse event (SAE) reports to the Safety Department within the time frame allotted by the Regulatory Department. Qualifications
An Associate of Nursing Degree; preferably Bachelor of Nursing Degree. Knowledge of medical and oncology research terminology and federal regulations, good clinical practices (GCP). At least one year of clinical nursing experience. At least one year of clinical research experience is preferred. At least one year of oncology nursing experience is preferred. Note: This section includes a link for applications and posting deadlines in the original text. For the refined description, this information has been consolidated to reflect the submission expectation and date: Interested candidates should submit their application through the SCRI careers page. Applications will be accepted through October 14, 2025. 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. SCRI focuses on advancing therapies for patients and has a broad research network across the U.S. Our Total Rewards package supports physical, mental, and financial well-being, including competitive compensation and benefits information through the parent company, McKesson. SCRI is an equal opportunity employer and values diversity, and does 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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As an Oncology Research Nurse at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will screen, enroll and follow oncology research study subjects, ensuring protocol compliance and close monitoring while patients are on the study. You are responsible for data collection, source documentation, and submission of adverse event reports. Responsibilities
You will support enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects. You will ensure the protection of study patients by timely adherence to protocol requirements and compliance. You will attend weekly study status teleconferences and monthly staff meetings. You will be familiar with the protocols on which the patients are enrolled, screen, treat, and follow patients. 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 (e.g., oral medication forms, pill count diaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws). 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; ensure medications, including antiemetics, are approved by the registrar prior to initiating treatment or when changing regimens (e.g., crossover studies). You will calculate the BSA, creatinine clearance, urine protein:creatinine ratio or other conversions 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 the process appropriately. You will accurately complete and submit follow-up serious adverse event (SAE) reports to the Safety Department within the time frame allotted by the Regulatory Department. Qualifications
An Associate of Nursing Degree; preferably Bachelor of Nursing Degree. Knowledge of medical and oncology research terminology and federal regulations, good clinical practices (GCP). At least one year of clinical nursing experience. At least one year of clinical research experience is preferred. At least one year of oncology nursing experience is preferred. Note: This section includes a link for applications and posting deadlines in the original text. For the refined description, this information has been consolidated to reflect the submission expectation and date: Interested candidates should submit their application through the SCRI careers page. Applications will be accepted through October 14, 2025. 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. SCRI focuses on advancing therapies for patients and has a broad research network across the U.S. Our Total Rewards package supports physical, mental, and financial well-being, including competitive compensation and benefits information through the parent company, McKesson. SCRI is an equal opportunity employer and values diversity, and does 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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