Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
The individual will be responsible for the designing, planning and execution of clinical pharmacology strategies & studies in support of development of small and large molecule drugs & cutting-edge novel modalities.
The Clinical Laboratory Scientist II ( CLS II ) functions with minimal direction from supervisory personnel. Responsibilities include blood and platelet collections, quality assurance audits in blood donor collections.
The Clinical Lab Scientist Coordinator performs chemical, microscopic, and/or bacteriologic tests and verifies results for use in the diagnosis and/or treatment of disease. This position also coordinates the technical operations of the laboratory sections for which responsible while also demonstrating competency in patient testing for neonate, pediatric, adult, and geriatric patients.
The Clinical Practice Coordinator (CPC) is an integral part of the Dignity Health Medical Foundation (DHMF) care team. The CPC performs the functions of assessing, planning, implementing and evaluating plans of care for attributed patients.
The Clinical Laboratory Scientist is responsible for performing moderately complex and complex laboratory tests, as defined by CLIA, in hematology, chemistry, urinalysis, microbiology, blood bank and serology.
The Clinical Research Nurse is a Registered Nurse (RN) who works collaboratively with physicians, Clinical Research Associates (CRA) and pharmacists to coordinate care for an assigned population of patients who are enrolled in to IRB clinical research trials.