- 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
- Merck (Sacramento, CA)
- …for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field ... within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial… 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
- Naval Education and Training Command (Port Hueneme, CA)
- …equipment, testing, and student counseling. You will conduct research and studies to identify new methodologies, technologies, and techniques to improve the ... to be filled. The course work must have included study in at least four of the following five...five areas: Learning theory, psychology of learning, educational psychology: Study of learning theories as they relate to the… more
- Sumitomo Pharma (Sacramento, CA)
- …Duties and Responsibilities** + Responsible for and lead all activities related to clinical study design from clinical study concept to clinical study ... complex decisions + Leads and drives strategy for clinical studies for assigned asset(s) within the Ophthalmology therapeutic area...reporting + Provide clinical input for and participate in study set up and design including data collection tools,… more