- Sumitomo Pharma (Sacramento, CA)
- …Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and ... and system work instructions. Provide support and guidance to study team members during the full lifecycle of the... team members during the full lifecycle of the study , including planning, set-up, maintenance, QC and closure of… more
- J&J Family of Companies (Irvine, CA)
- …you will be doing:** **Clinical Leadership** + Lead the support for all clinical studies - both for regulatory purposes as well as physician initiated collaborative ... studies . They will be responsible and accountable for case...for the development of materials to be used for study execution (investigator brochures, training materials, etc.) + Work… more
- Bristol Myers Squibb (San Diego, CA)
- …responsible for the design, implementation, monitoring, analysis, and reporting of studies conducted within RayzeBio's portfolio to ensure the program meets the ... and partner with investigators and CROs to design and implement clinical studies of radiopharmaceutical imaging agents. + Contribute to writing of protocols,… more
- AbbVie (Irvine, CA)
- …clinical studies and ensures scientific integrity and interpretation of study data from a clinical development program. Provides medical and/or scientific ... direction to project/ study teams. Should expect to be asked to participate...etc.) as they relate to planned and on-going clinical studies or projects. + Assists in scientific education of… more
- Charles River Laboratories (San Diego County, CA)
- …regular clinical rounds and routine health monitoring and examinations in support of studies and in accordance with the requirements of the research program, and ... As appropriate, recommend, administer, and record (following coordination with study directors) routine treatment of animals. Generate summary reports as… more
- Charles River Laboratories (South San Francisco, CA)
- …regular clinical rounds and routine health monitoring and examinations in support of studies and in accordance with the requirements of the research program, and ... being. As appropriate, recommend, administer, and record (following coordination with study directors) routine treatment of animals. Generate summary reports as… more
- Gilead Sciences, Inc. (Foster City, CA)
- …document review and data inclusion for NDA submissions of assigned studies by collaborating with cross-functional partners to meet clinical development project ... consultation on clinical development plans, clinical trial design and clinical study endpoints, calculating sample size, authoring statistical analysis plans and… more
- Bristol Myers Squibb (San Diego, CA)
- …responsible for the design, implementation, monitoring, analysis, and reporting of studies conducted within RayzeBio's portfolio to ensure the program meets the ... and partner with investigators and CROs to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study… more
- Gilead Sciences, Inc. (Foster City, CA)
- …approaches to optimize study parameters and interpret outcomes. + Prepare study protocols and coordinate execution of nonclinical studies which may involve ... responsibilities include designing and interpreting in vitro and in vivo studies , integrating data into mathematical models, and generating simulations to support… more
- Ascendis Pharma (Palo Alto, CA)
- …Associate Director ensures will be working on biostatistics deliverables, including study design, data analysis, data mining, epidemiology-related analyses, use of ... standards, specifications and datasets as needed + Contributes and reviews clinical study protocols, Case Report Forms (CRFs), and internal project plans for… more