RN Research Oncology
RN Research Oncology
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Overview
Responsibilities
Supports the regulatory process in the submission of study protocols consent forms and recruiting materials to the Institutional Review Board and the department for approval facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Helps coordinate activities for multiple simultaneous clinical trials managing various research tasks efficiently ensuring optimal use of resources and executing research protocols in a timely manner. Serves as study coordinator for pharmaceutical and/or device trials successfully coordinating site initiation visits monitoring visits and closeout visits and ensuring adherence to protocol guidelines and regulatory requirements.
Corresponds with healthcare teams providers outside research partners and patients ensuring clear communication and continuity of care for patients.
Assists in collecting and Reviewing data specific to clinical research studies to ensure accuracy and reliability. Assists with the maintenance of records of patient interactions and clinical research interventions to ensure consistent and coordinated care including collaborating with Investigator in assessment and management of Adverse Events.
Completes clinical tasks within the scope of nursing license to meet patients immediate needs as necessary. Coordinates patient care under direction of the Investigator and in accordance with the clinical trial protocol.
Attends Investigator meetings and conferences as required.
Performs other duties as assigned.
Qualifications
Preferred: Bachelors Degree in Nursing
Employment Type
Full-Time
