Clinical Laboratory Scientist, Oncology PM Shift BillionToOne IncClinical Laboratory Scientist, Oncology PM ShiftMenlo Park, CA$59.14–$67.29 / hourAt BillionToOne, we''ve built a category-defining, publicly traded company on Nasdaq where transparency fuels trust, collaboration drives breakthroughs, and every contribution moves the needle on our mission to make life-changing diagnostics accessible to all. Unity Confirm enables non-invasive confirmation for high-risk screening results through the capture of intact circulating fetal cells using BillionToOne's Fetal Cell Capture Technology.
Disease-focused Neuroscience and Translational Neurobiology Faculty Position | Gladstone Institutes and UCSF The J David Gladstone InstitutesDisease-focused Neuroscience and Translational Neurobiology Faculty Position | Gladstone Institutes and UCSFSan Francisco, California$250,000–$350,000 / yearA meaningful place to grow and learn –whether it’s your professional skills or scientific knowledge, we have the resources and environment to advance either so you can better support Gladstone’s mission to drive a new era of discovery in disease-oriented science and to mentor tomorrow’s leaders in an inspiring and excellent environment. To qualify for a faculty appointment at UCSF, applicants must possess a medical or doctoral degree, appropriate postgraduate or postdoctoral training, and at least four years of teaching/mentoring experience (during residency, fellowship, and/or in the lab) by the time the appointment becomes effective.
NewMedical Science Liaison-- Genetic Counselor - Rare Disease LabcorpMedical Science Liaison-- Genetic Counselor - Rare DiseaseSan Francisco, CaliforniaThis Medical Science Liaison (MSL) position will work within a diverse team of field-based MSLs and serve as a scientific and clinical expert between Labcorp Cardiology/Neurology and Rare disease business and key opinion leaders (KOLs), healthcare professionals (HCPs), major medical associations and academic centers through the dissemination, clarification and education of pertinent scientific and clinical information, primarily related to rare disease. Serve as an expert resource and provide educational support for the field sales group and other internal partners on Labcorp rare disease broad range of products including but not limited to Cardiology, Neurology, Immunology, rare disease and other panels included in our rare disease offerings.
NewSr. Pharmacovigilance (PV) Clinical Scientist SGA Inc.Sr. Pharmacovigilance (PV) Clinical ScientistSouth San Francisco, CA$49–$63.40 / hourMaintains robust knowledge of Technical Product Complaints (TPC) & Medical Product Complaint (MPC) for all company products including combination products Responsible for ensuring all product complaints are reported to the appropriate stakeholders within defined timelines. Ensures appropriate due diligence to obtain missing and/or additional information for Adverse Events (AEs) is performed in accordance with company SOPs / local and global regulations Escalates any issues pertaining to follow up activities and provide strategic resolution to USPS management.
Nurse Practitioner - Interventional Radiology UCSF Medical CenterNurse Practitioner - Interventional RadiologySan Francisco, CAPre-hospital clinical: Identifies potential patients through referrals, educates patients and families in their disease and treatment, evaluates patients through performing history and physical examinations and ordering laboratory tests, plans care in conjunction with Neuro IR physicians and other medical teams. Outpatient/Post hospitalization: Maintains communication with patients/families after discharge by telephone follow-up, fields inquiries from patients and outside caregivers and responds quickly and appropriately with the guidance of the Neuro IR physicians, maintains proper records on each patient.
Senior Embryologist UCSF Medical CenterSenior EmbryologistSan Francisco, CA$110,400–$235,400 / yearThis role works in collaboration with faculty, lab managers, clinic managers, and external stakeholders and agencies to participate and support research projects conducted by the faculty members in the division in support of the Reproductive Endocrinology and Infertility (REI) Division and the REI Research Group (REIRG), within the Department of Obstetrics and Gynecology. As part of UCSF''s mission of clinical excellence, education, research, and public service, Women''s Health leaders and teams work collaboratively to develop scalable solutions that improve care delivery, support strategic growth, and advance the health and well-being of women and families throughout California and beyond.
Assay Development - Research Associate 2 / Sr. Research Associate Personalis, IncAssay Development - Research Associate 2 / Sr. Research AssociateFremont, CA$85,000–$115,000 / yearOur products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Our full-time regular positions also include an annual performance-based bonus (or a sales incentive plan) and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the level and position offered.
Senior Clinical Study Manager Intuitive Surgical IncSenior Clinical Study ManagerSunnyvale, CAResponsible for the planning and execution of the clinical studies including site selection, analysis of potential patient recruitment and projections, creation of study related documents (protocols, case report forms, Informed consents, Clinical trial agreements, study reports), organizing IRB/EC submissions with follow-thorough to ensure successful progress. The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, develop clinical study reports, or support the development of clinical publications.
Process Engineering Associate I/Ii, Oncology BillionToOneProcess Engineering Associate I/Ii, OncologyMenlo Park, CA$75,029–$85,748 / yearThe PEA I is responsible for (1) developing new tools for improved clinical workflow efficiency, (2) analyzing process data to monitor and troubleshoot our high-throughput assays, 3) identifying root causes of recurring errors with proper documentation to enable long term corrective actions. At BillionToOne, we've built a category-defining, publicly traded company on Nasdaq where transparency fuels trust, collaboration drives breakthroughs, and every contribution moves the needle on our mission to make life-changing diagnostics accessible to all.
Associate Director, Project Management Alector IncAssociate Director, Project ManagementSouth San Francisco, CA$190,000–$220,000 / yearWe are supported in this mission by experienced and accomplished scientists and clinicians, a novel portfolio of programs, leading healthcare investors, and pharma company partners, who share in our commitment to bettering the lives of patients and realizing a world where we make brain disorders history. Reporting to the Head of Clinical Development, you will collaborate with leaders and subject matter experts across Research, Development, Clinical, Regulatory, CMC, and other functions to translate strategy into actionable plans, proactively manage risks, and accelerate program progress.
Process Engineering Associate I/II, Oncology BillionToOneProcess Engineering Associate I/II, OncologyMenlo Park, CA$75,029–$85,748 / yearThe PEA I is responsible for (1) developing new tools for improved clinical workflow efficiency, (2) analyzing process data to monitor and troubleshoot our high-throughput assays, 3) identifying root causes of recurring errors with proper documentation to enable long term corrective actions. At BillionToOne, we've built a category-defining, publicly traded company on Nasdaq where transparency fuels trust, collaboration drives breakthroughs, and every contribution moves the needle on our mission to make life-changing diagnostics accessible to all.
FSP - QC Reviewer Thermo Fisher Scientific IncFSP - QC ReviewerFoster City, CA$67,699–$80,000 / yearWithin our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With 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.
EHS SPEC 5 UCSF Medical CenterEHS SPEC 5San Francisco, CAConducts reviews of plans, specifications, calculations, Alternate Methods of Compliances (AMCs), Post Approval Documents (PADs) and other submittal documents for UCSF campus facilities' fire and life safety systems and construction requirements including, but not limited to, exiting systems, smoke removal systems, automatic fire/smoke detection and alarm systems, automatic fire sprinkler/suppression systems, fire resistive/rated building construction and all related fire and life safety work. Core program areas include biosafety, chemical safety, environmental protection, ergonomics, facilities safety, fire and life safety, industrial hygiene, radiation and laser safety, hazardous materials management, spill response, food facility safety, personal protective equipment (PPE) selection, hazardous building materials, and hazardous waste management, among others.
Nuclear Medicine Technologist Supervisor UCSF Medical CenterNuclear Medicine Technologist SupervisorSan Francisco, CAThe Nuclear Medicine Technologist Supervisor is licensed in all scopes of practice as defined by the State of California Radiologic Health branch and performs routine to complex diagnostic and therapeutic nuclear medicine procedures using radiopharmaceuticals to assist in diagnosis and/or treatment in both the inpatient and outpatient environment. 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.
Clinical Lab Scientist - Monogram Labcorp Holdings IncClinical Lab Scientist - MonogramSouth San Francisco, CA$52–$67 / hourOperate and maintain equipment and instruments according to manufacturer and Monogram established procedures including: analysis of clinical specimens, calibration, preventive maintenance, and troubleshooting. If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility.
Clinical Dietitian - Cardiovascular And South Asian Translational Heart Initiative Clinic Stanford Health CareClinical Dietitian - Cardiovascular And South Asian Translational Heart Initiative ClinicPalo Alto, CA$48.26–$62.73 / hourSpecialty certification granted by the Commission on Dietetic Registration Board, Certified Nutrition Support Specialist (CNSC), Certified Clinical Transplant Dietitian (CCTD) or Certified Diabetes Care and Education Specialist (CDCES). The Clinical Dietitian II functions independently at the competent to proficient level of the SOP/SOPP to provide nutrition care to patients, including complex patient types.
Associate Director, Medical Writing (SF Bay Area) Structure Therapeutics IncAssociate Director, Medical Writing (SF Bay Area)South San Francisco, CA$186,000–$235,000 / yearJob Responsibilities: Regulatory & Clinical Document Development: Lead the authoring, review, and finalization of high-quality regulatory and clinical documents, including Clinical Study Protocols, Clinical Study Reports, Investigator Brochures, Briefing Documents, CTD Module 2 summaries, and responses to regulatory agency information requests. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
Clinical Research Coordinator I – The Nallamshetty Lab PAVIRClinical Research Coordinator I – The Nallamshetty LabPalo Alto, CAFull timeQUALIFICATIONS Required: Bachelor's degree (or equivalent experience);Valid Driver License required;0-2 years of experience supporting clinical research, healthcare, laboratory, or related scientific environments;DesiredDegree in related field;Experience with grants and contracts function, clinical trial and research data management;Experience coordinating clinical research studies, recruiting research participants, collecting research data, and working with regulatory requirements;Knowledge of clinical research principles, Good Clinical Practice (GCP), human subjects protections, and research ethics gained through education or experience is desired. The position works closely with the Principal Investigator, study team, sponsors, regulatory bodies, and research participants to ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), institutional policies, and federal regulations.
Senior Manager Clinical Affairs Intuitive SurgicalSenior Manager Clinical AffairsSunnyvale, CAThis role will oversee and manages clinical protocols and other key study documents in support of regulatory submissions; manage clinical publications and evidence dissemination strategy, oversee manage communications with clinical trial sites, CROs, KOLs and medical societies; grow, develop and manage team to interface and support all clinical requirements of the company with the applicable guidelines and regulations; foresee challenges and develops critical concepts and methodologies to overcome those. As a key cross-functional constituent, this employee will work closely with functions across the organization - Regulatory Affairs, R&D, Program Management Office (PMO), Clinical Research Engineering (CRE), Clinical Research Managers, Global Access Value Economics (GAVE), Global Public Affairs (GPA), Regulatory Compliance, Training, Legal, and commercial functions to optimize clinical study strategies to meet business objectives.
NewMaterials Specialist Yowei TherapeuticsMaterials SpecialistMilpitas, CAIn 2004, CSBio opened a peptide production facility in Menlo Park, CA and in 2014, CSBio expanded production capability through the addition of a new, state of the art building dedicated to cGMP peptide production. Their work spans longevity and peptide therapeutics, clinical trials, evaluation of a 503A pharmacy model, personalized synthetic neoantigen peptide oncology programs, and supporting microbiology and laboratory capabilities.