- Cedars-Sinai (Los Angeles, CA)
- …we strive for. **What will you be doing in this role?** The Clinical Research Coordinator II works independently providing study coordination including screening ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- Cedars-Sinai (Los Angeles, CA)
- …The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- Cedars-Sinai (Los Angeles, CA)
- …Children's! To learn more, please visit:** Cedars-Sinai Guerin Children's. The Clinical Research Coordinator I works independently providing study coordination, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- Cedars-Sinai (Los Angeles, CA)
- …The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- Gilead Sciences, Inc. (Foster City, CA)
- … development project deliverables and timelines. + Provides input into, or otherwise leads, clinical trial protocol design, clinical study reports and health ... clinical development. You may also act as the Physician Responsible on certain projects. For the assigned projects,...Presents scientific information at scientific conferences as well as clinical study investigator meetings. + Adheres to… more
- Pfizer (South San Francisco, CA)
- …informed consent documents, and contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical ... for programs within the Late-Stage Oncology portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies maintaining current scientific… more
- Cedars-Sinai (CA)
- …per week. If hired you must reside in the commutable area.** The Clinical Research Coordinator II works independently providing study coordination including ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- Cedars-Sinai (CA)
- …The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, ... response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and… more
- Cedars-Sinai (Los Angeles, CA)
- …implement guidelines. **Qualifications** **Job Requirements** + A graduate degree in Physician Assistant studies from an accredited program. + Current ... a smooth transition back to a healthy lifestyle. Job Responsibilities As a Physician Assistant within our Colorectal Surgery department, you will: + Assist in… more
- J&J Family of Companies (Santa Clara, CA)
- …The Field Clinical Specialist will also play a critical role in clinical studies including device training, case support and ensuring timely data collection ... with a sense of urgency and drive. + Present clinical study training materials based on investigational...A history of effective collaboration with regulatory agencies through clinical studies and market releases. + Product… more