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Reporting to the Administrative Director, the Clinical Laboratory Scientist (CLS) Program Director is responsible for: all aspects of organization and administration of the Program; plans and directs school curriculum and daily activities; evaluates program effectiveness; assures compliance with all institutional, governmental, certifying and accrediting agencies; and organizes and directs the admissions process for the program.
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The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.
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Under supervision of the Clinical Research Manager of the Clinical Trials Unit, the Assistant Clinical Research Coordinator supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management of multiple Phase II-IV cancer-related protocols according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures.
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Demonstrated problem-solving, analytical, and multitasking skills with a good understanding of clinical research, statistical programming and CDISC standards. A technical and innovative role that partners with statistical programming, clinical analytics, data standards, statistical sciences, data sciences and information technology experts to implement next generation clinical data analysis ecosystem.
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Must be knowledgeable of Good Clinical Practices, protection of human subjects in research practices, and FDA regulatory guidelines regarding clinical research. Reporting to the Clinical Research Supervisor, Clinical Research Manager, or Director of Clinical Research Operations, the Clinical Research Coordinator II (CRC-II) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians, inter- and intradepartmental stakeholders, and sponsors.
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Current/unrestricted Licensed Clinical Social Worker (LCSW) or Licensed Professional Counselor (LPC) or Licensed Mental Health Counselors (LMHC) (or state equivalent) or Current Licensed Marriage and Family Therapists (LMFT only in CA.
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The Research Support Services (RSS) unit in SOM Deans Office / Finance Division works with SOM departments and units with its Pre-Award support needs, acting as the Pre-Award Contract and Grant Analyst for the department and PI, providing the coordination, preparation, budget development and routing of all SOM/RSS client department proposals for sponsored funding (except for industry initiated/funded clinical trials which are support by the Center for Clinical Research.
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The ideal candidate possesses at least a bachelor’s degree and a valid California Clinical Laboratory Scientist Generalist license with experience performing validations and data review for drug confirmation testing using liquid chromatography tandem mass spectrometry (LC/MS) methods.
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Working knowledge of design control procedures, design transfer to manufacturing, regulatory requirements, FDA, IEC, CE, ISO, IEEE. Provide engineering support to internal and external customers, including manufacturing, sales, clinical services, medical practitioners, and product users.
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FISI adheres to ISO and FDA regulations and operates dual cGMP manufacturing facilities in California, USA, and Tokyo, Japan. The company provides unrivaled service and quality to scientists working in biopharmaceuticals, cell therapy, regenerative medicine, assisted reproductive technology and cytogenetics, and industrial cell culture for the large-scale production of biotherapeutics and vaccines.
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Provide clinical support and supervision to MSW and/or MFT student interns as a designated Field Instructor. Reporting to a Clinical Supervisor, the Mental Health Therapist provides direct clinical and psychoeducational services to individuals (adults and minors), families, and groups.
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Basic Qualifications: Experience Minimum of one (1) year of experience as a Clinical Chaplain/Spiritual Counselor in a Hospital, Ambulatory, Home Health, Palliative Care or Hospice setting required.
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Under the general supervision of the Chief Clinical Laboratory Scientist, obtains and processes patient specimens and performs various clinical laboratory test for use in the diagnosis and treatment of disease.
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Experience with healthcare industry-specific interface standards and code sets (IHE, ANSI, HIPAA, SNOMED, etc.) Advanced knowledge of data integration tools, techniques and standards (e.g. HL7, IHE standards, Cloverleaf interface engine, etc.
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The School of Nursing and Health Professions seeks to hire part-time (adjunct) nursing faculty to assume teaching responsibilities for pre-licensure (undergraduate and ME-MSN) nursing students in a clinical setting.
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