- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... Deep knowledge of the drug development lifecycle, including preclinical and clinical stages, regulatory requirements, and quality standards. **Competencies**… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …true to the best of my knowledge. **Job Description** **About the role** As Associate Director , API Process Engineering, you will be Takeda's global expert for ... chemistry fundamentals to design, scale, and control API processes from clinical development through commercial supply. Through the integration of mechanistic… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... + Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial, and public domain information resources to identify relevant… more
- Gilead Sciences, Inc. (Foster City, CA)
- …aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs, you will act as the ... leaders and teams. + May participate on other Sub-teams (eg, Study Management, Clinical , Nonclinical, Biomarkers) or assign such to other colleagues and oversee and… more
- BeOne Medicines (Emeryville, CA)
- …estimate appropriate staffing levels that will enable the delivery of the BeOne clinical trial portfolio. Reporting to the Director of Global Resource ... algorithm development to model future resource demand for various roles within clinical development. The role will also focus on analyzing data and generating… more
- Amgen (South San Francisco, CA)
- …team. Join us and transform the lives of patients while transforming your career. Associate Director Scientist **What you will do** Let's do this. Let's change ... characterize drug-target interactions, leveraging microphysiological models to better predict clinical outcomes, and developing next level analytical techniques to… more
- Amgen (South San Francisco, CA)
- …Join us and transform the lives of patients while transforming your career. **Scientific Associate Director - PKDM (Small Molecule ADME)** **What you will do** ... preclinical study designs. + Contributing to the analysis of pre- clinical ADME and PK data for IND and NDA...the position. As an organization dedicated to improving the quality of life for people around the world, Amgen… more
- WuXi AppTec (San Diego, CA)
- …Inc. (US), a WuXi AppTec Company, is seeking a highly motivated and established Director with deep and broad expertise in Immunology drug discovery and research. The ... Director will lead the teams both in San Diego...projects to ensure successful execution of projects and best quality services. * Builds and grows a high-performance team,… more
- BeOne Medicines (San Mateo, CA)
- …analytics and systems, the Global Strategic Feasibility Analytics Lead collaborates with clinical development and clinical operations stakeholders to foster a ... of the studies, for early to late-stage medicines development across global clinical operations (GCO). Good understanding of global, regional, and country landscape… more
- Merck (Sacramento, CA)
- …enabled workflows. **Required Skills and Experience:** + Knowledge of manufacturing, testing, quality , and supply chain processes from late clinical development ... Under the guidance of dCMC Regulatory Authoring Leadership, the Associate Principal Scientist, Regulatory Authoring Business Owner, will optimize regulatory… more