- Bristol Myers Squibb (San Diego, CA)
- …radiopharmaceutical programs. This senior role is responsible for driving innovative research in novel isotope and chelator development , translating cutting-edge ... scientists and associates. + Documentation: Draft and review CMC sections for regulatory submissions, SOPs, and comprehensive development reports. + Travel: Less… more
- Genentech (South San Francisco, CA)
- …of CMC project deliverables. Key collaborators and interfaces include Quality, Genentech Research , Regulatory , other technical development functions, and ... collaborations with key partners, (eg,, Research , quality, regulatory , and other technical development functions and...development functions and teams) **Who you are** + PhD in chemistry, biochemistry, biology, or related field with… more
- Lilly (San Diego, CA)
- …institutions, and research organizations to enable the discovery and early development portfolio and strategy ** Regulatory & Medical Affairs Support** + ... pre-IND, IND submissions, interactions to ex-US health authorities, as well as regulatory strategy development + Monitor patient safety and ensure compliance… more
- Bristol Myers Squibb (Madison, NJ)
- …Stakeholder Engagement and Communication + Will work closely with colleagues in BMS Research , Development , Regulatory , Medical, Commercial and other key ... the field + Partner and interact with colleagues from Research and Early Development who design and...greater than 10 years of extensive clinical trial, drug development , and regulatory experience, in addition to… more
- AbbVie (Irvine, CA)
- …facial injectables, body contouring, plastics, skin care, and more. With our own research and development team focused on driving innovation in aesthetics, we're ... development subject matter expert, author, edit and review key section of research protocols, reports and regulatory submissions. Responsibilities: + Based on… more
- Pfizer (New York, NY)
- …indications. Typically, work on two to three clinical programs and support the development and provide consultation regarding multiple research projects. + Work ... on all Pfizer Oncology first-in-human clinical trials with input from Oncology Research Unit, Oncology Regulatory Strategy, Clinical Pharmacology and Precision… more
- Genentech (South San Francisco, CA)
- …Medical Director will have strong collaboration with cross-functional teams, including clinical research , regulatory affairs, and product development , to ... Clinical Development Plan (CDP) Strategy & Planning, CDP Execution, Regulatory Activities, and Cross-Functional Team Leadership. + You will mentor other… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …improvement skills, this individual will identify opportunities to streamline current development processes that comply with regulatory guidelines, with the ... improvement skills, this individual will identify opportunities to streamline current development processes that comply with regulatory guidelines, with the… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and with key internal partners (Quality, Legal, HPS) and scientific liaisons from Research and Development . Present and defend strategic positions to bring ... motivate others. + Experience managing and directing teams/vendors in process research / development , drug product formulations and clinical GMP CTM manufacturing.… more
- Amgen (Thousand Oaks, CA)
- …have the opportunity to support activities and represent SET on both Discovery Research and Early Development teams, providing functional area expertise. **Key ... lasting impact on the lives of patients as we research , manufacture, and deliver innovative medicines to help people...the lives of patients while transforming your career. **Process Development Sr Scientist** **What you will do** Let's do… more