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, including, but not limited to, multiple myeloma and acute myeloid leukemia using the Cytometry by Time of Flight (CyTOF) processing technique. Perform a variety of routine and non-routine laboratory research
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, including, but not limited to, multiple myeloma and acute myeloid leukemia using the Cytometry by Time of Flight (CyTOF) processing technique. Perform a variety of routine and non-routine laboratory research
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, including, but not limited to, multiple myeloma and acute myeloid leukemia using the Cytometry by Time of Flight (CyTOF) processing technique. Perform a variety of routine and non-routine laboratory research
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in manufactory sterilization process, knowledge about the standard of AAMI guidance and Extensive experience on embryonic stem cells, human and mouse T cells and hematopoietic stem cells handling
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data reporting requirements. Review and process invoices from sub-sites. Regulatory Responsibilities for Participating Sites: Manage deviation, adverse event, and unanticipated problem reporting. Systems
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for the management of the patient. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
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to treat patients with type 1 diabetes and further diabetes research. This position will require a flexible work schedule, including occasional weekend on-call hours. As a successful candidate you will
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. The successful candidate: Hours: Part time, Thursdays only (12hrs per week) Performs all tasks related to the EHR admission/discharge process of outpatient and inpatient visits. Performs accurate patient
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the process of ensuring all appointed medical staff meet requirements as outlined in Medical Staff By-Laws, CMS, TJC and any other external regulatory body. Manages multiple practice-related processes such as
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revising Standard Operating Procedures as necessary for cell product manufacturing and process development. · Cooperate with Quality Control (QC) and Quality Assurance (QA) groups to ensure