Maintaining and coordinating safety programs in a basic and clinical research setting; assisting with the development of safety literature / departmental process, research personnel support, support for incident response / investigation; provision of safety training, biosafety review of research projects, research area inspections / audit; coordinating multiple / simultaneous small scale projects for assigned user groups.
As a Medical Technologist III, staff can expect to perform (in accordance with standard operating procedures and applicable regulatory requirements) basic and advanced donor and patient tests, and interpret results to determine donor-recipient compatibility.
In this role, you will assist the Clinical Trials Office in association with the Associate Director of clinical services, in promoting and supporting all aspects of clinical research the Wilmot Cancer Center and affiliate hospitals including all treatment modalities.
In this role, you will be responsible for collecting, reviewing and completing preadmission information and securing related signoff. Effectively communicates with agency staff, medical team, patients and family throughout the discharge process to implement an effective treatment plan.
The Research Award Coordinator is responsible for coordinating, administering (financial and logistical), reporting as well as monitoring and tracking budgets for major research proposals at the ECE Department.