Senior Medical Director - Late Stage Revolution MedicinesSenior Medical Director - Late StageRedwood City, CaliforniaHas demonstrated collaborate behaviors on enterprise-level strategic initiatives with a variety of internal and external partners and stakeholders - including clinical investigators/clinicians, scientists and key opinion leaders (KOLs), as well as internal groups, including other groups in development, research, business development, commercial, legal, etc. Represent the clinical development plan on appropriate teams, sub-teams and forums; oversee training of study site personnel, act as primary point-of-contact for questions/enquires regarding the CDP at a program level, oversee the conduct of medical/safety data reviews and study reporting.
Senior Director, Translational Medicine Revolution MedicinesSenior Director, Translational MedicineRedwood 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. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Senior Director, Translational Medicine Revolution Medicines IncSenior Director, Translational MedicineRedwood City, CA$244,000–$305,000 / 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. This role will report to the Head of Clinical Biomarker Development and will be leading the design and execution of clinical biomarker plans for RAS(ON) inhibitor clinical programs across solid cancer types.
Medical Director Revolution MedicinesMedical DirectorRedwood City, California$295,000–$339,000 / yearHas demonstrated collaborate behaviors on enterprise-level strategic initiatives with a variety of internal and external partners and stakeholders - including clinical investigators/clinicians, scientists and key opinion leaders (KOLs), as well as internal groups, including other groups in development, research, business development, commercial, legal, etc. Represent the clinical development plan on appropriate teams, sub-teams and forums; oversee training of study site personnel, act as primary point-of-contact for questions/enquires regarding the CDP at a program level, oversee the conduct of medical/safety data reviews and study reporting.
Director, Program Management – Business Enablement AbbottDirector, Program Management – Business EnablementAlameda, CaliforniaKey projects may include (1) global website platforms for commercial and ecommerce sites (2) implementation of new AI tools that enhance customer service agent productivity and improve customer experience (3) building a roadmap that enables personalized marketing. General Medical Devices: Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ngersticks.
Senior Medical Director Maze TherapeuticsSenior Medical DirectorSouth San Francisco, CA$337,500–$412,500 / yearOur clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease. As a Senior Medical Director for one or more development programs, you will partner closely with cross-functional team members and other technical experts to design, conduct, and interpret the key clinical studies, including first-in-human and proof-of-concept trials.
Director, Medical Writing Maze TherapeuticsDirector, Medical WritingSouth San Francisco, CA$223,000–$271,000 / yearOur clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease. Lead the medical writing function and be accountable for the development of high-quality clinical and regulatory documents across Maze’s development programs, including protocols, clinical study reports, health authority meeting materials, and submission-supporting content.
Medical Director / Senior Medical Director Nurix Therapeutics IncMedical Director / Senior Medical DirectorBrisbane, CA$285,000–$390,000 / yearThis role will work cross-functionally and participate in the execution of clinical studies including protocols, provide scientific expertise to support site and CRA training, data cleaning/analysis, investigator interaction and support of regulatory filings. Advanced degree in clinical or biological sciences (MD, PhD, or PharmD preferred) 15+ years (Executive Director) relevant drug development experience with minimum of 5 years' experience in oncology clinical trials.
Medical Director / Senior Medical Director 5948-306 Nurix Therapeutics IncMedical Director / Senior Medical Director 5948-306Brisbane, CA$285,000–$390,000 / yearThis role will work cross-functionally and participate in the execution of clinical studies including protocols, provide scientific expertise to support site and CRA training, data cleaning/analysis, investigator interaction and support of regulatory filings. Advanced degree in clinical or biological sciences (MD, PhD, or PharmD preferred) 15+ years (Executive Director) relevant drug development experience with minimum of 5 years' experience in oncology clinical trials.
Sr/Exec Director, Quality Assurance GCP ErascaSr/Exec Director, Quality Assurance GCPSouth San Francisco, CAConduct gap analysis and risk assessment for critical study level activities that may impact subject safety and/or the quality and reliability of data, including but not limited to: Study Design and Protocol Requirements, Clinical Vendors and Service Providers-Transferred Obligations, contractual duties per SOW, and overall performance, Internal processes (e.g., vendor oversight), and Clinical Site and PI assessment and performance. Reporting to the Chief Operating Officer, the Senior or Executive Director Quality Assurance GCP will lead GCP activities and have responsibility for strategic and tactical oversight and implementation of QA GCP operations in support of Erasca's clinical development programs (Phase 1, 2, 3), regulatory submissions, and planned future commercial launches.
Director, Ambulatory Access & Revenue Operations Alameda Health SystemDirector, Ambulatory Access & Revenue OperationsSan Leandro, CA$72.52–$120.88 / hourDetermines access and revenue cycle impact and goals tied to performance; analyzes all existing reporting tools and develop data to establish performance goals; implements quality assessment and improvement initiatives; measures and reports performance internal and external customer satisfaction surveys and methods for rewarding evidence of progress and improvement; communicates goals to all levels of staff and regularly assesses achievement; collaborates with clinicians and services to advance revenue cycle improvements. + Develop and implement performance improvement activities across all primary and specialty care clinics in an effort of identifying areas of opportunities for improving patient care and financial outcomes, defines strategies to achieve enhancement, defines process and outcomes measures to monitor effectiveness of initiatives, and communicates to the health system.
Director, Product Management - Data Platform AsurionDirector, Product Management - Data PlatformSan MateoFluency with the modern data stack: Databricks (Delta Lake, Unity Catalog, MLflow), Snowflake, Amazon EMR/Spark, and cloud-native data services on AWS or GCP. Asurion — the world’s leading connected device protection company, serving 300M+ customers — is looking for a hands-on Director of PM to own the strategy and roadmap for our Data Platform.
Director, Cloud Operations (10364) Extreme NetworksDirector, Cloud Operations (10364)San Jose, California$250,000–$300,000 / yearFull timeWork authorization: We are unable to sponsor or take over sponsorship of an employment visa, including H-1B visas, at this time About the position: Extreme’s Cloud Operations team is a group of talented engineers passionate about building and operating highly reliable, scalable, and secure cloud solutions across public, private, and edge cloud environments. Even with 50,000 customers globally, including half of the Fortune 50 and some of the world's leading names in business, hospitality, retail, transportation and logistics, education, government, healthcare, and manufacturing, we remain nimble and responsive to ensure customer and partner success.
Director, System Test Skylo TechnologiesDirector, System TestMountain View, CA$215,000–$225,000 / yearEnvision, design, and scale Skylos worldwide system test architecture and lab strategy - maintaining hybrid test environments that span physical devices, satellite channel emulators, and cloud-based automation agents to enable thorough pre-production validation of NTN-specific behaviors. Our direct-to-device service is live on millions of activated devices across five continents, covering more than 72 million square kilometers, in partnership with leading satellite operators, mobile network operators, Tier-1 chipset makers, and OEMs worldwide.
Sr. Director, Drug Product Dev & Manufacturing (On-site) Corvus PharmaceuticalSr. Director, Drug Product Dev & Manufacturing (On-site)South San Francisco, CA$200,000–$250,000 / yearCoordinate with Quality and Supply Chain teams to ensure timely manufacture and release of drug product lots by leading technical reviews of batch records, deviations, change controls, and nonconformance investigations; proactively identify and mitigate risks related to clinical supply. Oversee technical activities at drug product CMOs, including technology transfer, clinical trial material (CTM) production, process troubleshooting, QbD and PAR studies, risk assessments, registration batch production, and process validation.
Director, CMC Project Management (Biologics) Enigma SearchDirector, CMC Project Management (Biologics)Redwood City, CaliforniaDrive multidisciplinary CMC teams, including cell line development, upstream and downstream process development, formulation development, analytical method development and qualification, drug substance and drug product manufacturing, quality control, regulatory filing, and supply chain management to maximize the value of development work and ensure effective communications and quality decisions. They are currently seeking a highly skilled and strategic Biologics CMC Project Manager to spearhead their chemistry, manufacturing, and controls (CMC) operations from Post-Candidate Selection (PCC) through IND submission.
Associate Director, Gxp Electronic Systems Quality Assurance Revolution Medicines, Inc.Associate Director, Gxp Electronic Systems Quality AssuranceRedwood City, CA$186,000–$233,000 / yearProvide strategic quality eadership for Computerized System Validation (CSV) and Computer Software Assurance (CSA), including risk-based validation approaches, system changes, upgrades, integrations, data migrations, and periodic reviews. Serve as the Digital Systems QA SME for regulatory inspections and audits, maintaining inspection readiness and monitoring evolving FDA, EMA, PMDA, GAMP 5, 21 CFR Part 11, EU Annex 11, data integrity, CSA, and AI-related regulatory expectations.
Director, Target Biology Revolution Medicines, Inc.Director, Target BiologyRedwood City, CA$211,000–$264,000 / yearWe are looking for an experienced drug hunter to lead the Target Biology team, provide hands-on scientific and people leadership, and work cross-functionally to identify and rapidly assess promising new targets, determine hit identification strategy, and advance screening hits through the early stages of hit-to-lead discovery. Work cross-functionally with partners in Medicinal Chemistry, Structural Biology, Discovery Biology, Translational Research, and Cancer Immunology to prioritize oncology targets, implement hit discovery plans, and drive progression from hit identification through lead generation.
Associate Director, Customer Engagement AkasaAssociate Director, Customer EngagementSouth San Francisco, CaliforniaSome of our recent recognitions include being named one of America's Top Startup Employers 2026 by Forbes, #1 most promising healthcare RCM startup of 2025 by Black Book Market Research, and one of the fastest-growing GenAI startups to watch by AIM Research. As the leading provider of generative AI solutions for the healthcare revenue cycle, we help health systems comprehensively capture and communicate the full patient clinical journey.
Director, Strategic Sourcing And Supplier Management Revolution Medicines, Inc.Director, Strategic Sourcing And Supplier ManagementRedwood City, CA$211,000–$264,000 / yearSupport cross-functional CRDMO management activities, covering all aspects such as business needs identification, market screening, contracting, vendor qualification and set-up, compliant delivery of services, and discontinuation. 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.