NewSenior Drug Discovery Scientist AxiomSenior Drug Discovery ScientistSan Francisco, CaliforniaPartner directly with drug hunters at top pharma companies, researchers at leading AI labs, and Axiom’s multidisciplinary team to build the experimental datasets and agentic systems needed to accurately predict human outcomes, then deploy those systems into real discovery workflows to inform major go/no-go decisions across high-value drug programs. In this role, they will work directly with great scientists at top pharma and biotech companies, researchers from leading AI labs, and Axiom’s multidisciplinary team to build the experimental datasets, agentic systems, and product capabilities needed to accurately predict human drug outcomes.
NewSenior Robotics Research Engineer, Robotics And AI For Drug Discovery NvidiaSenior Robotics Research Engineer, Robotics And AI For Drug DiscoverySanta Clara, CADeep comfort in working through the complexities of simulation and real-world robotics, including debugging physics simulators and renderers under rapid development; selecting, setting up, maintaining, and enhancing complex robotics hardware; debugging communication systems (latency, bandwidth, race conditions); and designing robust workflows for model training and evaluation. Collaborating with research scientists and engineers in the NVIDIA + Lilly Co-innovation AI Lab with deep expertise across a wide variety of fields (e.g., computational biology and chemistry, generative and agentic AI, bioinformatics, simulation).
Senior Robotics Research Engineer, Robotics and AI for Drug Discovery NVIDIA CorpSenior Robotics Research Engineer, Robotics and AI for Drug DiscoverySanta Clara, CADeep comfort in working through the complexities of simulation and real-world robotics, including debugging physics simulators and renderers under rapid development; selecting, setting up, maintaining, and enhancing complex robotics hardware; debugging communication systems (latency, bandwidth, race conditions); and designing robust workflows for model training and evaluation. Collaborating with research scientists and engineers in the NVIDIA + Lilly Co-innovation AI Lab with deep expertise across a wide variety of fields (e.g., computational biology and chemistry, generative and agentic AI, bioinformatics, simulation).
FSP - Scientist - Formulations, Drug Delivery Thermo Fisher ScientificFSP - Scientist - Formulations, Drug DeliverySouth San Francisco, CaliforniaWith clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Analytical Characterization: Independently analyze formulations using a diverse suite of analytical techniques (including spectroscopy, rheology, chromatography, calorimetry, light scattering, and physicochemical property measurements) to assess structure, composition, and physicochemical properties.
Scientist I OR Scientist II, DevOps Drug Substance, ONSITE, Fremont CA Boehringer Ingelheim International GmbHScientist I OR Scientist II, DevOps Drug Substance, ONSITE, Fremont CAFremont, CA$60,000–$122,000 / yearOperating as a DevOps DS project team member and occasionally as a team leader/coordinator, the incumbent applies scientific principles and process knowledge and expertise in cell culture and/or purification CMC development to execute, analyze, and document complex experiments with regular team interaction, and develop solutions to address frequently encountered problems. Operating as a DevOps DS project team member and occasionally as a coordinator, the incumbent applies scientific principles and process knowledge and expertise in cell culture and/or purification CMC development to execute, analyze, and document routine experiments with minimal oversight and complex experiments with regular team interaction.
Senior Director, Small Molecule Drug Discovery In Inflammation Discovery Amgen Inc.Senior Director, Small Molecule Drug Discovery In Inflammation DiscoverySouth San Francisco, CAIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. The Senior Director, Small Molecule Drug Discovery in Inflammation will provide strategic, and scientific leadership across Amgen's Inflammation Small Molecule Research portfolio, with accountability for advancing high-impact programs from early discovery through clinical and regulatory support.
Senior Director, Small Molecule Drug Discovery in Inflammation Discovery Amgen IncSenior Director, Small Molecule Drug Discovery in Inflammation DiscoverySouth San Francisco, CAIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. The Senior Director, Small Molecule Drug Discovery in Inflammation will provide strategic, and scientific leadership across Amgen's Inflammation Small Molecule Research portfolio, with accountability for advancing high-impact programs from early discovery through clinical and regulatory support.
Associate Director, Drug Substance Manufacturing - Upstream Process Vera Therapeutics Inc.Associate Director, Drug Substance Manufacturing - Upstream ProcessBrisbane, CA$175,000–$210,000 / yearWorking with the CMC team and other key functions such as project management, QA and Regulatory, the ideal candidate must be an outstanding leader with a proven track record of overseeing all drug-substance upstream manufacturing activities at the CMO site, including process scale-up, technology transfers, validations, PPQ campaign support, continuous process improvements, and post-approval lifecycle management of commercially approved products. The individual will serve as a subject matter expert (SME) in upstream processes for outsourced drug-substance manufacturing, technology transfer, life cycle management, and global regulatory submissions of complex Biologics, monoclonal antibodies, and other recombinant therapeutics.
Senior Director, Medical Safety & Pharmacovigilance Cytokinetics IncSenior Director, Medical Safety & PharmacovigilanceSouth San Francisco, CA$351,180–$409,710 / yearAs Senior Director, Medical Safety & Pharmacovigilance, this person will be responsible for oversight of PV and Drug Safety staff in managing the safety assessment of products, including review of individual and aggregate AEs, signal detection, preparation of safety reports, and risk management activities, and will work collaboratively with project teams and outside partners. Serve as the medical lead for signal detection and signal management activities, including identification, evaluation, interpretation, and communication of emerging safety signals through review of individual case reports, aggregate safety data, clinical trial data, literature, and external sources.
Associate Group Director, Quantitative Safety Sciences F. Hoffmann-La Roche LtdAssociate Group Director, Quantitative Safety SciencesSouth San Francisco, CARole models Roche Values and Leadership Commitments while providing effective leadership to an experienced global team of Quantitative Safety Scientists across multiple locations; sets team direction in terms of remit, emphasis, style, behaviours, and culture while driving, embedding, and supporting staff to adhere to agreed organisational models, mindsets, and new ways of working. Establishes an internal and external connected network to anticipate future opportunities, understand stakeholder needs/ideas, and promote collaborative projects (e.g., PSI, Clinical Safety, PD Data Science, pRED/gRED) while leading/contributing to global cross-functional initiatives and PDS strategic projects to define and implement SAR and PVSD priorities.
Patient Safety & Pharmacovigilance Case Management Operations Lead Corcept TherapeuticsPatient Safety & Pharmacovigilance Case Management Operations LeadRedwood City, CA$209,100–$340,000 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Strong expertise in safety database systems (e.g., Argus) and electronic reporting requirements, including demonstrated success with drug safety case processing combined with a thorough knowledge of drug safety database utilization, systems and applications.
Associate Group Director, Quantitative Safety Sciences Hoffmann-La Roche LtdAssociate Group Director, Quantitative Safety SciencesSouth San Francisco, CARole models Roche Values and Leadership Commitments while providing effective leadership to an experienced global team of Quantitative Safety Scientists across multiple locations; sets team direction in terms of remit, emphasis, style, behaviours, and culture while driving, embedding, and supporting staff to adhere to agreed organisational models, mindsets, and new ways of working. Establishes an internal and external connected network to anticipate future opportunities, understand stakeholder needs/ideas, and promote collaborative projects (e.g., PSI, Clinical Safety, PD Data Science, pRED/gRED) while leading/contributing to global cross-functional initiatives and PDS strategic projects to define and implement SAR and PVSD priorities.
Safety Operations Physician Revolution Medicines IncSafety Operations PhysicianRedwood City, CA$261,000–$300,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Analyze quality and compliance metrics, perform root cause analyses for identified issues, and help drive corrective and preventive actions in partnership with GPS Quality and cross-functional stakeholders.
Senior Director, Safety Biostatistics Ideaya Biosciences IncSenior Director, Safety BiostatisticsSouth San Francisco, CA$270,000–$334,000 / yearThe Senior Director of Safety Biostatistics will be a leader of Biostatistics and Biometrics at IDEAYA and will oversee and provide strong statistical support to the development of IDEAYA therapeutics in close collaboration with Clinical Development, Regulatory Affairs, Data Management, Program Management, and especially with focus with Drug Safety and Pharmacovigilance. Non-Solicitation Policy and Notice to Agencies and Recruiters: IDEAYA's Non-Solicitation Policy strictly prohibits agencies and recruiters from any contact and communication with IDEAYA employees, managers, and leaders to submit unsolicited candidate resumes and/or to solicit business partnerships.
Assoc Business Development Director - Safety Solutions IQVIA Holdings IncAssoc Business Development Director - Safety SolutionsSan Francisco, CA$89,900–$250,400 / yearResponsibilities include full cycle sales including: target identification, securing and managing client meetings, listening and understanding client needs, addressing client concerns/objections, managing Subject Matter Experts in defining opportunities, proposing solutions, negotiating, obtaining SOWs and closing the deal. The Associate Business Development Director works collaboratively with other colleagues to increase sales of IQVIA's Safety and Regulatory services and technology within the life sciences industry.
Safety Operations Physician Revolution MedicinesSafety Operations PhysicianRedwood City, CaliforniaLeveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Analyze quality and compliance metrics, perform root cause analyses for identified issues, and help drive corrective and preventive actions in partnership with GPS Quality and cross-functional stakeholders.
Senior Safety Scientist II Revolution Medicines, Inc.Senior Safety Scientist IIRedwood City, CA$186,000–$233,000 / yearThe Opportunity:The Senior Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.
Clinical Safety Program Lead Abbott LaboratoriesClinical Safety Program LeadSanta Clara, CA$114,000–$228,000 / yearThe ideal candidate brings a unique blend of clinical research operations experience, project management expertise, and clinical or medical knowledge, enabling them to lead complex studies, evaluate safety data, influence cross-functional decision-making, and provide strategic guidance throughout the clinical development lifecycle. A key focus of the role is supporting ongoing priority studies while leading execution of upcoming IDE clinical investigations, ensuring consistent, inspection-ready delivery and successful clinical development outcomes across the portfolio.
Senior Safety Scientist II Revolution MedicinesSenior Safety Scientist IIRedwood City, CaliforniaThe Opportunity: The Senior Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.
Senior Safety Scientist II Revolution Medicines IncSenior Safety Scientist IIRedwood City, CA$186,000–$233,000 / yearThe Opportunity: The Senior Safety Scientist within Global Patient Safety Science is an individual contributor who provides safety science and pharmacovigilance support to all products across the RevMed portfolio, which includes early and late phase development activities. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.