The US Oncology Network
Location
Norfolk, Virginia
The role involves screening and enrolling patients for cellular therapy trials and managing the informed consent process. Additionally, the nurse maintains regulatory documents and collaborates with physicians to ensure protocol compliance and patient safety.
Candidates must be a graduate of an accredited nursing program with at least one year of nursing experience, preferably in oncology. Current RN licensure in Virginia and BCLS or ACLS certification are required.
Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research RN to support our office in Norfolk. ***Please take this quick survey once you've submitted your resume to complete the application process: Clinical Research PI Link ****If you have completed the survey before, even for another position, please do not take it again.
Present trial concepts, objectives and treatment details to potential patients for various cellular therapy trials, while conducting detailed assessment and screening to determine their eligibility. Participating in the informed consent process and enrolling patients on protocol 80% of the job will be computer based, and direct patient care is limited in a non-RN Clinical Research Coordinator role Collects and maintains regulatory documents in accordance with USOR SOP and applicable regulations. Participates in scheduling monitoring and auditing visits, as well as interacting with the monitors/auditors while onsite. Coordinating patient care in compliance with protocol requirements Collaborating with the physician to review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to drug study and thoroughly documenting all findings Working directly with other research bases and/or sponsors Overseeing the preparation of orders by physicians to assure that protocol compliance is maintained Communicating with physicians regarding study requirements, need for dose modification and adverse event reporting
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