- University of Southern California (Los Angeles, CA)
- …prior to CIC approval, looking specifically at necessity and feasibility of required study tests, at areas pertaining to patient compliance, dose modification and at ... or effort to facilitate budget set up.2. Ensures that study is conducted as written so that scientific questions...of the stamped Informed Consent. Answers patient's questions regarding study and toxicities. c. Calculates correct dose of drug… more
- University of Southern California (Los Angeles, CA)
- …support to investigators in the development of research protocols for a project or study . Or supervises a segment of a research project such as data collection or ... data analysis. + Contributes to the documentation and update of study procedures. Coordinates design, revision, approval and production of research instruments and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …program-related activities. These activities include, but are not limited to, study protocol preparation, additional study or investigator documentation, ... contributions to data analysis plans, study reporting, and clinical development inputs into regulatory documentation, publications and scientific presentations.… more
- The County of Los Angeles (Los Angeles, CA)
- …of cases, including identifying treatment outcomes. + Obtains and studies medical, psychological, social, and family histories by interviewing individuals, ... of psychological evaluations. + Initiates and carries out psychological research studies and provides rationale to implement departmental or service programs;… more
- The County of Los Angeles (Los Angeles, CA)
- …department at the level of Senior Regional Planner*.One year of graduate study in an accredited college with specialization in Planning, Environmental Studies ... from an accredited college/university with a specialization in Planning, Environmental Studies , Geography, Urban Studies , Public Administration, or Landscape… more
- Stanford University (Stanford, CA)
- …regulations, help to develop standard operating procedures for veterinary care and study implementation, help research staff design and implement in vivo studies ... Assist in the design and implementation of in vivo studies * Complete reports as required for research ...studies * Complete reports as required for research studies * May perform tasks associated with other teams… more
- Cedars-Sinai (Los Angeles, CA)
- …budget and research subject informed consent documents are consistent. + Monitors study payments and generates invoices as necessary to ensure adequate funding ... financial disclosures, FDA forms, CVs, medical licenses, etc.) for research studies . + Completes appropriate IRB paperwork and submits internal and external… more
- University of Southern California (Los Angeles, CA)
- …case reviews for all potential encounters generated from transplant patients and time studies for both staff and physicians/surgeons. The TCS is responsible for the ... however it is appropriate. + 7. Responsible for overall management of time study collection process for staff, physicians and surgeons ensuring all applicable time … more
- Actalent (Alameda, CA)
- …candidate will independently coordinate clinical supply activities for clinical studies , aiding the development programs. Key activities include reviewing clinical ... study protocols, designing clinical labels, preparing packaging and labeling...of Interactive Voice/Web response systems for use in clinical studies . + Working knowledge of GMP/GCP/GLP regulations required. Additional… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Success in this role requires excellence in design and conduct of epidemiologic studies /analyses, direct expertise in use of RWE at different stages of the product ... of clinical outcomes, comparative safety and effectiveness research, and post-approval safety studies . + Communicate effectively about the utility of RWE across the… more