116 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"CESBIO" positions at City of Hope
Sort by
Refine Your Search
-
demographic and insurance information at every registration and provides exceptional customer service in a fast‑paced Emergency Department environment. Key responsibilities Completing registrations for multiple
-
maintenance of data and source documentation. The CRN collaborates with Investigators in review of subjects’ recruitment and pre-screening for protocol eligibility. The CRN is responsible for developing
-
, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management
-
therapy. For more information about Dr. You’s lab, please visit here. As a successful candidate, you will: Lead and sustain an independent research program focused on hematologic malignancies, aligned with
-
the development of new processing procedures. Maintain laboratory supply inventories, operate within electronic Laboratory Information Management System (LIMS) and related software, and assist with administrative
-
Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. Collects necessary data to ensure
-
and procedures associated with managing the production of research animal breeding colonies, including mating, weaning, animal identification, tissue biopsy, data collection, and communication with
-
methods. Independently evaluate research data and initiate alternative approaches to improve the quality of results by providing input to overall research design that maximizes samples or refines the use
-
career development. For more information about Dr. You’s lab, please visit here. As a successful candidate, you will: Lead independent and collaborative projects investigating the molecular and cellular
-
involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory