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Research Nurse Coordinator-Office of Clinical Research
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Full-time
professional certificate
Posted 16d ago
~40 hrs/week
Responsibilities
Oversees daily operations of oncology clinical trials, including study coordination, regulatory compliance, and data management. Collaborates with research teams and sponsors to ensure protocol requirements and regulations are met.
Requirements
Requires a Registered Nurse license in Tennessee and at least two years of clinical oncology or related experience. Must have knowledge of Federal Regulations for Human Subjects, GCP guidelines, and hold BLS certification.
Full job description
Market Range: 12
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS:
The Research Nurse Coordinator- Oncology oversees the daily operations of the oncology clinical trials, including study coordination, regulatory compliance, IRB activities, data management, and research oversight under the direction of the Principal Investigator. This position collaborates with research teams, sponsors, and participants to ensure studies are conducted in compliance with applicable regulations and protocol requirements while supporting overall clinical trial operations within the Clinical Trials Unit.
Related keywords
OncologyClinical TrialsIRBGood Clinical PracticeGCPCITI Human Subjects ProtectionIATA Hazardous Materials ShippingHIPAABLSRegistered NurseClinical ResearchHuman Subjects Research
About University of Tennessee, Knoxville, Graduate School
A dynamic, innovative, collaborative partner in shaping graduate education and a dedicated advocate for attracting and developing a diverse student population.
Offices: 111 Student Services Building, Knoxville, Tennessee 37996, US · 201 Student Services Building, Knoxville, TN 37996, US
A dynamic, innovative, collaborative partner in shaping graduate education and a dedicated advocate for attracting and developing a diverse student population.
Offices: 111 Student Services Building, Knoxville, Tennessee 37996, US · 201 Student Services Building, Knoxville, TN 37996, US