- Cedars-Sinai (Los Angeles, CA)
- …field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, ... all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB)....quality and study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board… more
- Rincon Consultants (Los Angeles, CA)
- …to QA/QC processes to support technical accuracy and consistency **Client Coordination & Regulatory Support** + Serve as a point of contact for clients, agencies, ... across disciplines to align environmental review with client goals and regulatory expectations **Team Collaboration & Business Development** + Mentor junior staff… more
- Rincon Consultants (Oakland, CA)
- …the preparation and review of environmental documents, technical studies, and regulatory compliance materials. + Develop and oversee permitting strategies and ... consultations (FESA/CESA). + Foster collaboration across Rincon's environmental planning, regulatory , and biological resources teams to deliver integrated solutions.… more
- Merck (San Diego, CA)
- …engagements. This includes the ability to: + Solid knowledge of clinical research regulatory requirements (eg, GCP and ICH) + Ability to manage multiple competing ... skills **Education/Experience** Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR… more
- Gilead Sciences, Inc. (Foster City, CA)
- …RWE and application of adequate and contemporary analytical methods across drug development, including pediatrics and post-authorization phase of the product ... to: patient registries, studies of natural history of disease, drug utilization studies, studies of patient reported outcomes, comparative effectiveness/safety… more
- Medtronic (Northridge, CA)
- …testing, and authoring clear, concise, and well-structured reports to support regulatory submissions. The Senior Product Engineer applies scientific rigor in ... including the preparation of technical protocols and reports, as well as drug compatibility studies related to biocompatibility evaluations. The role also supports… more
- Fresenius Medical Center (Riverside, CA)
- …philosophy. Adheres to the FVC/FMCNA Compliance Program, including following all regulatory and FVC/FMS policy requirements. Provides direct nursing care pre, during ... + Responsible for supporting and driving FVC quality standards through meeting regulatory and accrediting body requirements and the practice of Continuous Quality… more
- Cardinal Health (Sacramento, CA)
- …hours. We also provide customers the support they need in regulatory compliance, reimbursement, continuing education, information management and other crucial areas, ... to support Cardinal Health customers, the scientific development of radiopharmaceutical drug products, and medical education. This role leverages internal product… more
- Stanford University (Stanford, CA)
- …Specific studies include evaluation of novel monitoring devices and both investigational drug and device studies focusing on novel treatments for acute kidney ... milestones, and invoice sponsors according to study contract. + Ensure regulatory compliance. Regularly inspect study document to ensure ongoing regulatory… more
- Stantec (Roseville, CA)
- …and support project teams that assist Stantec's clients to meet safety regulatory requirements and maintain effective management systems. Your Key Responsibilities - ... compliance programs - Supporting performance of environmental, health and safety regulatory compliance and program audits - Interacting with project managers, EHS… more