- 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
- BeOne Medicines (San Mateo, CA)
- …provide strategic statistical leadership for pharmacokinetic (PK) and pharmacodynamic (PD) studies across all phases of clinical development. This role partners ... Clinical Biomarker, Regulatory Affairs, and Clinical Development to ensure robust study design, insightful data analysis, and timely support for global regulatory… more
- Cedars-Sinai (Los Angeles, CA)
- …to assist in tasks supporting the coordination/implementation of noncomplex research studies . Supports objectives of research studies through noncomplex tasks ... to assist in tasks supporting the coordination/implementation of noncomplex research studies . + Collects, evaluates and/or abstracts clinical research data. May… more
- Avispa Technology (Palo Alto, CA)
- …primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. * Determine eligibility of and ... gather consent from study participants according to protocol. Assist in developing recruitment...Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case… more
- Cedars-Sinai (Beverly Hills, CA)
- …schedule. 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