Clinical Scientist / Neuropsychological Rater (Mandarin Bilingual) - Bay Area Irvine Clinical ResearchClinical Scientist / Neuropsychological Rater (Mandarin Bilingual) - Bay AreaOakland, CA$80,000–$90,000 / yearFull timeEmpirical Case Building & Advocacy: Synthesize diagnostic data and clinical history to build objective, evidence-based cases for protocol eligibility, advocating for complex or nuanced candidates who qualify under protocol criteria. Preferred Experience: Prior psychometrician or clinical rater experience in pharmaceutical clinical trials (specifically in Alzheimer’s Disease, MCI, or Major Depressive Disorder) is preferred and qualifies for higher starting compensation.
Clinical Scientist / Neuropsychological Rater (Bilingual Mandarin) Irvine Clinical ResearchClinical Scientist / Neuropsychological Rater (Bilingual Mandarin)Oakland, CA$80,000–$90,000 / yearEmpirical Case Building & Advocacy: Synthesize diagnostic data and clinical history to build objective, evidence-based cases for protocol eligibility, advocating for complex or nuanced candidates who qualify under protocol criteria. Preferred Experience: Prior psychometrician or clinical rater experience in pharmaceutical clinical trials (specifically in Alzheimer’s Disease, MCI, or Major Depressive Disorder) is preferred and qualifies for higher starting compensation.
Director, Clinical Development Alto NeuroscienceDirector, Clinical DevelopmentMountain View, CA$215,000–$255,000 / yearThe role requires a professional degree (MD, DO, NP, PA or PharmD), strong medical knowledge, excellent communication skills, and the ability to collaborate effectively with cross-functional teams and external sites, including clinical operations, regulatory affairs, and other departments to support the successful execution of clinical studies. This position involves confirming patient eligibility, assessing adverse events, interpreting clinical trial data, and ensuring that protocols are followed, patients are properly cared for, and all regulatory requirements are met.
Head of Project Management - CNS/Neuroscience (US/EU) Novotech Health Holdings Pte LtdHead of Project Management - CNS/Neuroscience (US/EU)South San Francisco, CA$200,000–$290,000 / yearTake a leading role in growing the CNS/ Neuroscience Therapeutic Area's book of business through working closely with the Medical & Scientific Strategist (MSS) and Business Development Team to develop successful operational strategies and delivery plans for project Proposals; participate in Bid Defense Meetings and lead operational follow up activities either personally or by overseeing the work of Portfolio Directors, Project Oversight Directors and/or Project Delivery Directors. This role requires outstanding leadership, highly developed strategic vision and energy to grow the book of business of the Therapeutic Area; operational expertise and the ability to effectively motivate the team of Portfolio Directors, Project Oversight Directors, Project Delivery Directors and Project Managers working in the Therapeutic Area to successfully achieve their goals.
Senior Manager, Imaging Vendor Partnerships, Clinical Development Edwards LifesciencesSenior Manager, Imaging Vendor Partnerships, Clinical DevelopmentSan Jose, CA$139,000–$196,000 / yearFrequently interacts with customers, and/or functional peer group managers, normally involving matters between functional areas, other company divisions or units, or customers and the company; often leads a cooperative effort among members of a project team. + Demonstrated ability to manage one or more teams and provide coaching and feedback, including responsibility for all employee actions including attracting, developing, and retaining talent and partnering with HR on all aspects of talent development.
Director, Clinical Quality & Compliance HeartFlowDirector, Clinical Quality & ComplianceSan Francisco, CA$215,000–$270,000 / yearThe Director will work closely with internal Clinical Operations teams and cross-functional partners to support and monitor compliance, ensure adherence with FDA IDE requirements and Good Clinical Practice (GCP), and maintain inspection readiness across all studies, both internally managed and externally initiated or managed. Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis).
NewClinical Manager - Home Health Sequoia Home Health and HospiceClinical Manager - Home HealthMilpitas, CaliforniaThe Pennant Group, Inc. is a holding company of independent operating subsidiaries that provide healthcare services through home health and hospice agencies and senior living communities located throughout the US. The Clinical Manager oversees home health clinical operations, ensuring high-quality patient care, regulatory compliance, and effective care coordination.
Surgical Services Clinical Manager Sutter HealthSurgical Services Clinical ManagerCastro Valley, CA$209,185.60–$334,692.80 / yearTotal compensation considers multiple factors, including, but not limited to a candidate's experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs. Develops and maintains a solid partnership with internal and external peers, leaders, and/or local/state/federal agencies to facilitate and collaborate on initiatives or issues resolution.
Clinical Nurse Manager, Medical Surgical Sutter HealthClinical Nurse Manager, Medical SurgicalSan Francisco, CaliforniaRegular Employees of Sutter Health and its entities may handle hazardous drugs in the course of their work, including patient care, which requires them to manage, store, prepare, receive, unpack, transport, dispose of, or administer drugs identified as hazardous or potentially hazardous by the National Institute for Occupational Safety and Health (NIOSH) and in accordance with the USP 800 guidelines. Total compensation considers multiple factors, including, but not limited to a candidate’s experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs.
Clinical Supervisor (BCBA) Center for Autism and Related DisordersClinical Supervisor (BCBA)Fremont, CaliforniaRemoteConstantly position oneself to participate and respond to the movements and behaviors of patients, including but not limited to bending to assist a patient, kneeling/crouching to teach a play skill, hurrying to block an open doorway, or reaching to prevent a patient from entering a traffic congested street. This includes the assessment and analysis of the patient’s skills and challenging behaviors, development of treatment plans, overseeing the implementation of treatment, collaboration with and training of their patient’s caregivers, as well as ongoing coaching and training of behavioral technicians.
Clinical Supervisor II Center for Autism and Related DisordersClinical Supervisor IIFremont, CaliforniaRemote$82,000–$122,000 / yearConstantly position oneself to participate and respond to the movements and behaviors of patients, including but not limited to bending to assist a patient, kneeling/crouching to teach a play skill, hurrying to block an open doorway, or reaching to prevent a patient from entering a traffic congested street. This includes the assessment and analysis of the patient’s skills and challenging behaviors, development of treatment plans, overseeing the implementation of treatment, collaboration with and training of their patient’s caregivers, as well as ongoing coaching and training of behavioral technicians.
Associate Director, Clinical Development Program Management Lyell Immunopharma IncAssociate Director, Clinical Development Program ManagementSouth San Francisco, CA$190,000–$230,000 / yearThis individual works closely with Core Team Leads, Clinical Development, CMC, Regulatory Affairs, Biometrics, Quality, Pharmacovigilance, and external partners (CROs/vendors) to ensure trials and programs are delivered on time, within budget, and in compliance with GCP and applicable regulatory requirements. Support cross-functional Program/Sub-Teams, driving alignment on scope, timelines, budget, and risk across Clinical Operations, CMC, Regulatory, Biometrics/Data Management, Quality, Pharmacovigilance, Medical Affairs, and Finance.
Join Our MedTech Talent Pool - Engineers, Scientists, Clinical, and R&D Experts T45 LabsJoin Our MedTech Talent Pool - Engineers, Scientists, Clinical, and R&D ExpertsSanta Clara, CaliforniaCandidates based in the Bay Area are generally expected to work in our Santa Clara office at least one day per week to support in-person collaboration and team activities. T45 Labs and its affiliated companies are committed to fair and equitable pay practices and may also consider additional compensation elements such as bonuses, equity, and benefits as part of the total rewards package.
Join Our Medtech Talent Pool - Engineers, Scientists, Clinical, And R&D Experts T45 LabsJoin Our Medtech Talent Pool - Engineers, Scientists, Clinical, And R&D ExpertsSanta Clara, CACandidates based in the Bay Area are generally expected to work in our Santa Clara office at least one day per week to support in-person collaboration and team activities. T45 Labs and its affiliated companies are committed to fair and equitable pay practices and may also consider additional compensation elements such as bonuses, equity, and benefits as part of the total rewards package.
NewClinical Lab Scientist Generalist Sutter HealthClinical Lab Scientist GeneralistOakland, CA$66.36–$82.88 / hourKnowledge of laboratory test methods, specimen requirements, test limitations, test interpretations sufficient to perform tests accurately and to recognize and analyze problems effectively. Position Overview: This position may be required to perform tests in all areas of the Clinical Laboratory including, but not limited to: Blood Bank, Hematology, Chemistry, Coagulation, Urinalysis and limited Microbiology.
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.
NewClinical Lab Scientist, Generalist Sutter HealthClinical Lab Scientist, GeneralistOakland, CA$66.36–$82.88 / hourBachelor's: from four-year college or university; and one year training or equivalent combination of education and experience meeting state requirements from four-year college or university; and one year training or equivalent combination of education and experience meeting state requirements. Knowledge of laboratory test methods, specimen requirements, test limitations, test interpretations sufficient to perform tests accurately and to recognize and analyze problems effectively.
Medical Director/Senior Medical Director, Clinical Development Tenvie Therapeutics IncMedical Director/Senior Medical Director, Clinical DevelopmentBrisbane, CARemote$270,000–$360,000 / yearThis physician leader will drive successful clinical trial execution, provide medical oversight, and support regulatory submissions partnering closely with cross-functional colleagues to advance differentiated therapies for patients with high unmet medical need. Tenvie Therapeutics is developing precision‑engineered small molecule therapies to address core drivers of neurological and peripheral diseases: neuroinflammation and cellular dysfunction.
Clinical Adjudicator, RN MaximusClinical Adjudicator, RNSan Francisco, CAFull timeMaximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. - Perform other special projects not related to a specific case such as general legal research, general medical research, drafting proposal sections, or acting as a liaison for a specific project, when necessary.
Regulatory Affairs Manager – Heart Failure (on-site) AbbottRegulatory Affairs Manager – Heart Failure (on-site)Pleasanton, California$114,000–$228,000 / yearAs an individual contributor, the function of a Regulatory Affairs Manager is to combine knowledge of scientific, regulatory and business issues to enable products that are developed, manufactured or distributed to meet required legislation. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.