Protocol coordination including subject recruitment, enrollment, implementation, and follow-up of appropriate research protocols for the Clinical Trials Office of OncologyPromote good clinical practice in the conduct of research possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protectionCompletion of CITI Training modules designed to educate staff on good clinical practices involving human subject researchContribute to clinic wide multidisciplinary tumor boards to seek out potential clinical trial candidatesCoordination of patient care, charting and communication.Collected, processed, and properly packaged and shipped specimens following strict preparation guidelinesCollected fresh biopsies from guided CT scans for participants in clinical trialsPreformed ECGs and blood draws on participantsRetained inventory on kits provided by 20 or more protocolsAbstract medical information from various sources in the patient medical record.Report adverse events to medical monitor, FDA, and all other governing bodies.Coordinate external audits and monitoring visits, and serve as liaison between institution and sponsor.

Compile and maintain record and bookkeeping, as well as managing the upkeep of business license applicationsCoordinating lesson plans for studentsCreate educational materials to further demonstrate subject matterMaintain a quiet and orderly workspaceEstablish a friendly, encouraging and welcoming environmentPromote high standards for academic

Assist in Animal Studies, Code, Transcribe, and/or Enter Data, Data Collection, Literature SearchUndertake basic research for example by preparing, setting up, conducting and recording the outcome of experiments and fieldwork

Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations.Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines.Protocol coordination including subject recruitment, enrollment, implementation, and follow-up of appropriate researchprotocols for the Cardiology Department.Promote good clinical practice in the conduct of research possessing knowledge of federal regulations and guidance documentsfor the conduct of clinical trials and human subject protectionPreparing, setting up, conducting and recording the development of questionnaires and conducting surveysContribute to the production of research reports and publications as well as conducting literature and database searches Contribute to the production of research reports and publications as well as conducting literature and database searchesManaging, collecting, coding and analyzing data obtained from research.Provide support to Principal Investigators.