UCSF Medical CenterToxicology Management Specialist (San Francisco, CA) UCSF Medical CenterToxicology Management Specialist (San Francisco, CA)San Francisco, CAMinimum of 2 years of experience in clinically-oriented pharmacy practice OR 2 years prior Poison Control Center experience or an equivalent combination of education and experience; and knowledge and ability necessary for the successful performance of the duties assigned to the position. The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.
UCSF Medical CenterToxicology Management Specialist (Madera, CA) UCSF Medical CenterToxicology Management Specialist (Madera, CA)San Francisco, CAPost graduate or clinical pharmacy residency or fellowship trainingAAPCC Certification as a Specialist in Poison Information or as a Diplomate of the American Board of Applied ToxicologyInvolvement in scholarly activitiesMultilingualPrior emergency medicine or critical care clinical pharmacy experienceExperience with study design, study data analysis, and manuscript preparationFormal teaching experience of clinical learners. Minimum of 2 years of experience in clinically-oriented pharmacy practice OR 2 years prior Poison Control Center experience or an equivalent combination of education and experience; and knowledge and ability necessary for the successful performance of the duties assigned to the position.
Exponent Inc.Principal Toxicologist (Ph.D.) Exponent Inc.Principal Toxicologist (Ph.D.)Oakland, California$200,000–$300,000 / year
LanceSoft IncNewScientist LanceSoft IncScientistFremont, CAFull timeProtocol Development: Author robust study protocols, develop data analysis/calculation worksheets, and execute benchtop laboratory testing in strict accordance with approved protocols. The generation of these experimental results will directly support the compilation of technical performance chapters for regulatory dossiers, ensuring compliance with the European Union's In Vitro Diagnostic Regulation (IVDR).
Bristol-Myers Squibb CoNewExecutive Director, Global Program Lead, Early Development Oncology - Targeted Therapies Bristol-Myers Squibb CoExecutive Director, Global Program Lead, Early Development Oncology - Targeted TherapiesBrisbane, CA$286,310–$346,945 / yearEach leader is accountable to therapeutic area, R&D, commercial and Company Leadership for: (i) creating a vision and defining the strategy and integrated development plan for each asset within their portfolio, (ii) developing a set of objective criteria against which each asset advancing through the pipeline will be evaluated to enable robust debate and rapid, data-driven decision making; and (iii) ensuring that only high quality and differentiated assets enter the market. Uses an understanding of disease biology, the drug development process (particularly cross-functional connectivity), and relevant late-stage challenges (e.g., trends in disease area therapeutic advances, and evolving regulatory, patient advocacy and market access environments) to create a vision for each asset, then design and execute effective development programs in support of the overall R&D portfolio goals.
Bristol-Myers Squibb CoNewSenior Dir, In-Vivo & Non-Clinical Pharmacology Bristol-Myers Squibb CoSenior Dir, In-Vivo & Non-Clinical PharmacologyBrisbane, CA$252,640–$306,137 / yearThis leader will partner deeply with Research leadership and the Pharmacology, DMPK, Toxicology, and Translational Science units to deliver the applications, workflow capabilities, AI, and supporting data flows that enable non-clinical decisions across in-vivo biology, DMPK, ADME, non-clinical safety, toxicology, and bioanalytical science. Non-clinical pharmacology generates the evidence that determines which candidates enter humans, and this role matters now because scientists need better integrated applications, AI, and workflows to generate, interpret, and act on that evidence with greater speed and confidence.
Star TherapeuticsAssociate Director, Translational Science Star TherapeuticsAssociate Director, Translational ScienceSouth San Francisco, CA$156,000–$195,000As an Associate Director, the candidate is expected to represent translational sciences as a translational medicine lead for clinical studies and work closely with the clinical development team members including bioanalysis, clinical operations, regulatory affairs, quality, medical writing, safety, clinical research and clinical leadership. As part of the collaborative research team role, the candidate is expected to work with individuals across research and translational research groups, including discovery research, drug development and protein sciences, preclinical bioanalysis and other junior staff within translational research organization.
Geosyntec Consultants, Inc.NewPrincipal Environmental Risk Assessor Geosyntec Consultants, Inc.Principal Environmental Risk AssessorOakland, CaliforniaThis position is ideal for an accomplished leader in toxicology, ecological risk assessment (ERA), and human health risk assessment (HHRA) who can help grow and lead complex site investigation, remediation, and redevelopment projects across industrial, energy, and public-sector markets. The role emphasizes technical leadership on CERCLA, RCRA, PFAS, sediment, vapor intrusion, and risk-based cleanup projects; trusted advisory relationships with clients and regulators; and collaboration across multidisciplinary teams.
Deep OriginVP/SVP of Drug Discovery Deep OriginVP/SVP of Drug DiscoverySan Francisco, CAThis individual will serve as a key scientific and operational leader inside the company, partnering closely with computational scientists, experimental scientists (own lab), platform teams, translational biology, external collaborators, and executive leadership to prioritize programs, guide strategic decisions, and accelerate pipeline execution. This is a critical executive leadership role for a hands-on scientific leader who has spent significant time navigating the realities of drug discovery and development — someone who understands not only what can work scientifically, but what actually translates into successful therapeutic programs.