In this role, the selected candidate will create experimental test designs, performs the assay testing on the VITROS analyzers, analyses the experimental data, and summarizes the results aimed for the development of new VITROS in vitro diagnostic products or processes using established protocols and SOPs.
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.
The User Research Analyst is responsible for designing, conducting, analyzing, and reporting on user tests to inform game design and drive impactful improvements in the usability and playability of Ubisoft titles.
In this role, you will assist project managers with method troubleshooting through data interpretation, experimental design and data collection ; and act as a technical resource for project managers in other troubleshooting efforts.
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, the selected candidate will perform various assignments related to the experimental design, testing, and analysis of assay testing on the VITROS analyzer systems in the laboratory in accordance with cGMP regulations.
The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Principal responsibility is the synthesis, purification, and identification of chemical intermediates and target compounds
The Research Programmer II will be tasked with clinical oversight of research staff related to specific testing and analysis in mathematical and computational modeling as part of the General Research Institute Center for Translational Systems Biology and Computational Medicine.
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.
The successful candidate must possess demonstrated expertise in both theoretical and experimental aspects of semiconductor quantum light sources, as well as experience in the engineering design of such structures.
The incumbent will provide general administrative support for the Research Program by: scheduling and providing logistical support for meetings, research rounds, and program events; drafting, formatting and editing correspondences.
the role will provide administrative support to the Vice Chairs, the Director of CPPD and Alumni, and the Director of Faculty Development, including participating on committees by taking minutes and coordinating logistics for meetings.