Under general supervision of a physician and or senior management, is responsible for the supervision of the clinical research program in a practice. Responsible for supervising clinical research coordinators and other research staff. Ensures site research quality by practicing in compliance with US Oncology Research, Inc (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations.
Supervises treatment research staff and regulatory staff. RN, BSN, CCRP, and OCN preferred. Strong computer skills in Excel, Access and Electronic Medical Records. Several years of supervisory and regulatory experience required. Must be familiar with code of federal regulations.
Minimum Qualifications: Associates degree in a clinical or scientific related discipline desired, graduate of an accredited nursing program preferred. Minimum of 5-7 years nursing experience, clinical or scientific related discipline, preferably in oncology. Supervisory experience preferred. Current licensure as a registered nurse in the state of practice preferred. Current BCLS or ACLS certification required for nurses. SoCRA or ARCP certification preferred.
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