Senior Product Manager - Samd (Hybrid) CeribellSenior Product Manager - Samd (Hybrid)Sunnyvale, CA$149,000–$192,000 / yearRegulatory Expertise: Extensive knowledge of regulatory processes for, software, hardware and AI-driven medical devices, specifically FDA 510(k) submissions and 21 CFR 820.30 design controls, with direct ownership of design control deliverables through a full product development lifecycle. The Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country.
Digital Clinical Lead Massachusetts General Physicians OrganizationDigital Clinical LeadBelmont, CaliforniaThe MGB Digital Clinical Lead (DCL) to McLean and system Behavioral and Mental Health (BMH) will provide leadership for the implementation of Digital solutions that enhance the clinician experience, while accounting for the delivery of high quality, safe, equitable, efficient care in an environment of exceptional patient experience. Busch, MD, MS, Mass General Brigham Assistant Chief Medical Information Officer for McLean Hospital and Behavioral and Mental Health, McLean Hospital, 115 Mill Street, Belmont, MA 02478, Email: abusch@mclean.harvard.edu and the Registrar and Professional Staff Office at rpsomclean@mgb.org.
CarT Nurse Epic CareCarT NurseEmeryville, California$65–$89 / hourSCOPE: The Infusion Nurse – Cellular Therapy and Clinical Research (full-time) is responsible for the safe and compliant administration of investigational and commercial therapies, including cellular therapies (e.g., CAR-T), within an outpatient oncology setting. The role may involve frequent exposure to clinical hazards such as communicable diseases, bodily fluids, hazardous substances, ionizing radiation, and various medications typically present in a healthcare environment.
Sr Product Manager, Ion Endoluminal Intuitive Surgical IncSr Product Manager, Ion EndoluminalSunnyvale, CAOperating with moderate independence on complex, multi‑stakeholder initiatives, the Product Manager provides strategic input into portfolio and roadmap development, translates voice‑of‑customer and field insights into actionable product requirements, and crafts compelling, data‑driven product narratives to influence tradeoff decisions and stakeholder alignment. Working across multiple product franchises and geographies, and in close partnership with R&D, Product Operations, Manufacturing, Clinical, Quality, Regulatory, and Commercial teams, this role serves as the central point of contact for downstream product management as well as bringing field insights into upstream investigations.
Sr Product Manager - Ion Systems Intuitive Surgical IncSr Product Manager - Ion SystemsSunnyvale, CAOperating with moderate independence on complex, multi‑stakeholder initiatives, the Product Manager provides strategic input into portfolio and roadmap development, translates voice‑of‑customer and field insights into actionable product requirements, and crafts compelling, data‑driven product narratives to influence tradeoff decisions and stakeholder alignment. Working across multiple product franchises and geographies, and in close partnership with R&D, Product Operations, Manufacturing, Clinical, Quality, Regulatory, and Commercial teams, this role serves as the central point of contact for downstream product management as well as bringing field insights into upstream investigations.
Phlebotomist / Administrative Assistant One Medical of NY, PCPhlebotomist / Administrative AssistantSan Francisco, CA$26.25–$28.25 / hourWhat you'll likely work on: Use impeccable C-I-CARE (a framework containing the key elements of a great interaction and effective communication that we use with patients and each other) in all patient interactions, both clinical and administrative, and ensure a fluid and positive in-office experience through patient intake, same day schedule management, appropriate follow up scheduling, strong knowledge of billing and insurance, monitoring patient feedback and assisting with outreach as necessary. Continue to care for our members beyond the lab room by answering patient messages, following up on lab cases and assisting our providers and virtual medical team with clerical duties such as, but not limited to biometric screening forms, medical record and consult review, billing inquiries, and DOH reporting.
Vice President, Clinical Development Ardelyx IncVice President, Clinical DevelopmentNewark, CA$360,000–$455,000 / yearThe Vice President, Clinical Development will initially serve as a highly hands-on individual contributor responsible for advancing ongoing and planned clinical programs, with a particular focus on supporting pediatric development activities in gastroenterology and broader pipeline initiatives. Position Summary: Reporting to the Chief Medical Officer, the Vice President, Clinical Development will play a critical role in shaping and executing Ardelyx's clinical development strategy across current and future pipeline programs.
Staff Clinical Development Engineer - Incubator Intuitive Surgical IncStaff Clinical Development Engineer - IncubatorSunnyvale, CAWorking closely with physicians and cross-functional partners, you will translate clinical and technical insights into structured development plans, drive execution of clinical and preclinical evaluations, and ensure that key risks are identified and resolved. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).
Regional MyoPro Specialist - PT/OT Only - Remote in Northern CA Myomo IncRegional MyoPro Specialist - PT/OT Only - Remote in Northern CACARemote$90,000–$135,000 / yearBased on patented technology developed at MIT, Harvard Medical School and by the Company, Myomo develops and markets the MyoPro product line of lightweight, non-invasive, powered arm braces (orthoses) to restore function in paralyzed or weakened arms and hands of individuals that have suffered a stroke, spinal cord, or nerve injury. Myomo is headquartered in Burlington, Massachusetts, with sales and clinical professionals across the U.S. What we're looking for: The Regional MyoPro Specialist drives and supports the referral program through product education, training, and support of various referral sources to meet business growth targets.
Vice President, Development Sciences (Clinical Pharmacology & Nonclinical) Lycia TherapeuticsVice President, Development Sciences (Clinical Pharmacology & Nonclinical)South San Francisco, CA$295,000–$350,000 / yearBuild the clinical pharmacology and nonclinical development function with the requisite scientific, safety/toxicology, PK/ADME, clinical pharmacology and regulatory expertiseOwn clinical pharmacology strategy across the pipeline, including PK/PD modeling, exposure-response analysis, and dose/regimen selection for first-in-human and later-stage clinical trials, integrating relevant nonclinical data. Direct experience in clinical pharmacology, including population PK/PD modeling and simulation, exposure-response analysis, and dose/regimen selection to support IND-enabling and later-stage clinical trials; experience authoring clinical pharmacology sections of regulatory submissions and interacting with FDA/health authorities on clinical pharmacology matters.
Senior Director, Real World Data RWD Freenome IncSenior Director, Real World Data RWDCARemote$236,300–$335,475 / yearAbout this opportunity: As the Senior Director of Real World Data (RWD), you will be accountable for defining, developing, and implementing our RWD strategy, platform, and data pipeline to transform diverse real-world datasets into regulatory-grade, research-ready assets that drive our clinical development, evidence generation, digital health products and product offerings. Specifically, the Senior Director will lead the RWD Informatics team in turning electronic health records (EHR), claims, imaging, and other RWD sources into research-ready datasets accessible by our biostatisticians,computational scientists and other end users while ensuring data quality, operational efficiency, and scalability.
Senior Human Factors Research Engineer Intuitive Surgical IncSenior Human Factors Research EngineerSunnyvale, CAThis role is a unique engineering and scientific opportunity with the expectation that knowledge and skills can be applied to experimental behavioral research that actionably informs product design strategies for future development, inform product development, and establish product claims with state-of-the-art human-robot interfaces. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).
Senior/Staff/Principal Backend Engineer, Platform & Data Ingestion Verana HealthSenior/Staff/Principal Backend Engineer, Platform & Data IngestionSan Francisco, CA$150,000–$236,000 / yearVerana Health, a digital health company that delivers quality drug lifecycle and medical practice insights from an exclusive real-world data network, recently secured a $150 million Series E led by Johnson & Johnson Innovation- JJDC, Inc. (JJDC) and Novo Growth, the growth-stage investment arm of Novo Holdings. Within the Oncology Platform, your work directly impacts patient care by dictating how fast and how cleanly raw medical documentation is unlocked and structured to support life-saving research and improving clinical outcomes.
Associate Director, Regulatory Affairs - Strategy Revolution Medicines, Inc.Associate Director, Regulatory Affairs - StrategyRedwood City, CA$186,000–$233,000 / 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. The candidate must have a thorough understanding of oncology drug development, applicable regulations, and current health authority thinking and be able to provide clear and concise feedback to management and project teams, facilitate decision-making and provide effective leadership to ensure successful regulatory outcomes.
Senior/Staff/Principal Backend Engineer, Platform & Data Ingestion Verana Health IncSenior/Staff/Principal Backend Engineer, Platform & Data IngestionSan Francisco, CA$150,000–$236,000 / yearVerana Health, a digital health company that delivers quality drug lifecycle and medical practice insights from an exclusive real-world data network, recently secured a $150 million Series E led by Johnson & Johnson Innovation - JJDC, Inc. (JJDC) and Novo Growth, the growth-stage investment arm of Novo Holdings. Within the Oncology Platform, your work directly impacts patient care by dictating how fast and how cleanly raw medical documentation is unlocked and structured to support life-saving research and improving clinical outcomes.
Sr Manager/Assoc Director, Process Dev & Mfg Erasca IncSr Manager/Assoc Director, Process Dev & MfgSouth San Francisco, CA$180,000–$215,000 / yearPosition Summary: Reporting to the Executive Director, Process Development and Manufacturing, the Senior Manager or Associate Director, Process Development and Manufacturing is a hands-on technical contributor responsible for designing and executing experiments that support process development and for coordinating and providing technical oversight of contract development and manufacturing organizations (CDMOs). The Senior Manager or Associate Director may serve as the drug substance lead for one or more programs and works independently and collaboratively to plan, execute, interpret, and communicate process development and manufacturing activities across internal and external teams.
Principal Product Manager, Real World Evidence Intelligence Revolution Medicines, Inc.Principal Product Manager, Real World Evidence IntelligenceRedwood City, CA$211,000–$264,000 / yearRequired Skills, Experience and Education: 12+ years of experience in Product Management, Data Product Management, RWE Informatics, Life Sciences Data Platforms, Evidence Strategy, Epidemiology, HEOR Analytics, Outcomes Research, or related roles within biotech, pharma, healthcare technology, consulting, data providers, or another regulated environment. The Opportunity: We are seeking a Principal Product Manager, Real-World Evidence Intelligence to shape products and capabilities that help teams use real-world data to design better studies, evaluate feasibility, support regulatory and evidence strategies, communicate value, and monitor outcomes across the product lifecycle.
Project Manager Clinical Affairs eTeam Inc.Project Manager Clinical AffairsSunnyvale, CARemote$87–$88 / hourAs a key cross-functional partner, this role will collaborate closely with Regulatory Affairs, Quality Compliance, Program Management, Clinical Affairs, Post-Market Surveillance, Regulatory Compliance, Training, Legal, and other stakeholders to strengthen inspection readiness, support compliance execution, and enable achievement of business and clinical quality objectives. Partner with internal stakeholders to develop internal processes, KPIs and drive identified initiatives, Support the development and execution of a proactive, risk-based clinical quality and compliance program that safeguards participant safety, supports data integrity, and promotes continuous improvement across all clinical studies.