- Pfizer (South San Francisco, CA)
- …investigator brochures, clinical study reports, statistical analysis plan, and regulatory documents. + Provide leadership to early stage clinical scientists ... with other clinicians, statisticians, clinical pharmacologists, translational biologists and regulatory specialists. Meet regularly with the Pfizer Oncology group… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Development, Device Development and Clinical Package Engineering, Quality Assurance, Regulatory , Outsourced Manufacturing and Project Management partners to develop ... and supports the resolution of CAPAs . Partner with Regulatory to ensure labels meet global regulatory ...Experience Requirements:** Requires a Bachelor's degree preferably in a science -related field 8+ Years with BA/ BS OR 6+… more
- AbbVie (Irvine, CA)
- …develop, and optimize new methods and techniques. Contribute to project science in area of expertise. Develop productive collaborations and communications with ... other groups across science disciplines. Responsibilities: + Design and provide scientific oversight of preclinical PK/TK studies + Conduct data analyses including… more
- Edwards Lifesciences (San Diego, CA)
- …year experience working in medical writing, medical affairs, clinical affairs and/or clinical science ; OR + Doctorate degree ( PhD , MD, PharmD) with relevant ... inspiring journey. As a key member of the Clinical Science team, the Specialist, Medical Writing is responsible for...Medical Writing is responsible for supporting the development of regulatory and clinical documents for a dynamic portfolio of… more
- Gilead Sciences, Inc. (Foster City, CA)
- …external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements, and environmental, health, and safety legislations. This ... collaboration at the Team Leadership level with the Development, Quality, Regulatory , Analytical, Supply Chain, and Product & Portfolio Strategy organizations within… more
- Terumo Neuro (Aliso Viejo, CA)
- …California, USA **Department Name:** 650-Clinical Admin-Post Market **Qualifications:** 1. PhD in Data Science , Biostatistics, Epidemiology, Bioinformatics, or ... actionable insights. Support the development of evidence packages that inform regulatory strategies, publications, and broader business objectives. Contribute to the… more
- Medtronic (Irvine, CA)
- …This role is ideal for a candidate who combines deep expertise in polymer science with a strong enthusiasm for artificial intelligence (AI) and data analytics to ... and resume._ + Requires a Baccalaureate degree in Polymer Science , Materials Science , or a related field...level of understanding of the medical device industry and regulatory requirements for Class II and Class III devices… more
- J&J Family of Companies (Irvine, CA)
- …https://www.jnj.com/. The Staff Clinical Research Scientist will join the Clinical Science & External Research (CSER) Team responsible for global evidence ... clinical landscapes, and a thorough understanding of publication standards, regulatory guidelines, and clinical study design. **Key Responsibilities:** + Develop… more
- Abbott (Alameda, CA)
- …than 160 countries. Abbott is a global healthcare leader, creating breakthrough science to improve people's health. We're always looking towards the future, ... anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you...or approval. **Preferred** + A master's degree or a PhD is ideal. + Experience in the medical device… more
- AbbVie (Irvine, CA)
- …in aesthetics, we're committed to providing the most comprehensive science -based product offerings available. The Director (II) Product Development, Global ... product portfolio, as well as in providing consultation/guidance to the Operations Science & technology, on technical issues on marketed products. This role will… more