Senior Research Associate, NGS - Genomics Platform (Fixed-Term Contract) Arc InstituteSenior Research Associate, NGS - Genomics Platform (Fixed-Term Contract)Palo Alto, CA$84,250–$114,250 / yearYou will work closely with scientists across Arc to coordinate sequencing submissions, perform sequencing operations, ensure rigorous quality control, and help maintain efficient, reliable production workflows across multiple next-generation sequencing platforms. Our two Institute Initiatives reflect this model in action: Virtual Cell Initiative : Building a full-stack virtual cell model to identify disease mechanisms and nominate drug targets, accelerating the path from biological insight to clinical trials.
Senior Research Associate, HPC Production (Fixed-Term Contract) Arc InstituteSenior Research Associate, HPC Production (Fixed-Term Contract)Palo Alto, CA$84,250–$114,250 / yearIn this role, you will serve as a dedicated producer of hematopoietic progenitor cells (HPCs), differentiating both parental and genetically edited human stem cells to supply high-quality HPCs for downstream research across multiple Tech Center teams. You will routinely execute staggered weekly rounds of HPC production, working ahead of demand by coordinating with requesting teams, scaling each round to meet projected needs, and maintaining the reagent and consumable stocks required to keep production uninterrupted.
Clinical Trials Manager - II Integrated Resources, IncClinical Trials Manager - IIFoster City, CaliforniaContractorIn partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines. Clinical Trials Manager - IIMust meet all requirements for Principal Clinical Research Associate position and have demonstrated proficiency in all relevant areas.
Clinical Trials Manager Integrated Resources, IncClinical Trials ManagerFoster City, CaliforniaContractorClinical Trials ManagerIn partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines. Provide input to program budget and timelines to ensure successful management of all aspects of international clinical trials.
Clinical Trials Manager II Integrated Resources, IncClinical Trials Manager IIFoster City, CaliforniaContractorIT Life Sciences Allied Healthcare CRODIRECT # - (650)-399-0891Gold Seal JCAHO Certified for Health Care Staffing"INC 5 0 0 0 's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row) In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
Field Research Supervisor UCSF Medical CenterField Research SupervisorSan Francisco, CAThe incumbent may have central responsibility for ensuring IRB approval and compliance, contract generation, negotiation and approval, subject recruitment, appropriate study testing, and adequate enrollment of multicenter clinical trials, longitudinal cohort studies, local investigator-initiated studies, and biorepository efforts. Partnering with Program Managers across the Division, the Supervisor ensures projects are accurately represented and appropriately prioritized, and coordinates with the finance team on budget management, monthly invoice review, and participant-reimbursement oversight.
Associate Scientist, Oncology Research CytomX Therapeutics IncAssociate Scientist, Oncology ResearchSouth San Francisco, CA$115,000–$135,000 / yearHeadquarters Location: South San Francisco, CA, Company relocating to Emeryville, CA Fall of 2026. Associate Scientist, Oncology Research.
Senior Research Associate Karius IncSenior Research AssociateRedwood City, CA$88,200–$102,900 / yearBy unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide. The company's platform is already delivering unprecedented insights into the microbial landscape, providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood, and helping industry accelerate the development of therapeutic solutions.
Senior Research Associate, Neural Cell Production (Fixed-Term Contract) Arc InstituteSenior Research Associate, Neural Cell Production (Fixed-Term Contract)Palo Alto, CA$84,250–$114,250 / yearOur two Institute Initiatives reflect this model in action: Virtual Cell Initiative : Building a full-stack virtual cell model to identify disease mechanisms and nominate drug targets, accelerating the path from biological insight to clinical trials. Produce stem cell-derived cell types for ADI such as neural progenitor cells (NPCs), neurons, astrocytes, and microglia, reliably and consistently, following established differentiation protocols.
Research Associate AccuraGenResearch AssociateMilpitas, CAYou will assist in experimental design, data collection, and analysis while collaborating with scientists to advance our MRD assay. Ensure accurate and consistent recording of experiment methods, materials and results; keep a high-quality laboratory notebook.
Research Associate II, Konermann Lab Arc InstituteResearch Associate II, Konermann LabPalo Alto, CAThis is a Research Associate II position in the Konermann Lab at Arc Institute and the Stanford Medical School Department of Biochemistry, working closely with a scientist in the lab to identify the key pathways that drive the progression of neurodegenerative diseases using advanced CRISPR technologies and functional assays. Our two Institute Initiatives reflect this model in action: Virtual Cell Initiative : Building a full-stack virtual cell model to identify disease mechanisms and nominate drug targets, accelerating the path from biological insight to clinical trials.
Clinical Data Associate III Integrated Resources, IncClinical Data Associate IIIFoster City, CaliforniaFull timeEssential Duties and Job Functions: Works collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists, Biomarker Statistical Programming group, Biomarker Biostatistics group, Biomarker Clinical Programming group, Biobanking and Sample Management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting. Knowledge, Experience and Skills: 3 years of experience and a BS degree.1 year of experience and a MS degree or PhD.Qualifications1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience2) Project management experience of clinical trials3) Understanding of clinical data management processes4) Communication with cross-functional study team members
Sr. Research Associate/Associate Scientist, Nonclinical Development Adicet BioSr. Research Associate/Associate Scientist, Nonclinical DevelopmentRedwood City, CaliforniaAdicet is located in a state-of-the-art facility and works to create an incredible office experience with an onsite gym and various other fitness options, onsite parking with electric vehicle charging stations and free shuttle (Caltrain), company-subsidized lunches (delivered onsite daily) and fully stocked breakrooms. Coordinate and execute in vivo and ex vivo nonclinical studies to evaluate Adicet’s immune-cell and gene-therapy platforms, including efficacy, pharmacokinetic/pharmacodynamic, and safety assessments in relevant murine oncology and immunology models.
Research Scientist - I Integrated Resources, IncResearch Scientist - IHayward, CaliforniaFull timeMust demonstrate hands on experience in cell-culture methods, blood based assays, cellular assays, immunoassays, bead based assays and flow cytometry or microscopy methods.•Good understanding/application of fluorescence based probes/approaches including antibodies, dyes etc.•Must demonstrate ability to design and conduct experiments, analyze data, interpret results and present findings with minimal supervision.•Strong collaborative and independent decision making skills.•Proficiency in Microsoft Office (Word, PowerPoint, Excel) required - experience with statistical analysis) preferred. KNOWLEDGE, SKILLS & ABILITIES:•Creative and versatile scientist with broad scientific experience.•Strong analytical and organizational skills, confidence, versatility and initiative•Excellent written and verbal communication skills.•Ability to work in a fast-paced, multi-tasking, team-oriented environment.•Strong troubleshooting and problem solving skills.•Be able to travel to collaborator sites.
Staff Research Associate UCSF Medical CenterStaff Research AssociateSan Francisco, CAExample: 25% Essential/Yes - Administration: Under general supervision, oversee all aspects of the administrative office; Interact with university officials, faculty, staff and representatives from outside agencies; Assist in the preparation and coordination of Federal and non-federal grant applications from initial submission to annual progress reports; Prepare and track purchasing and payment authorizations. We are currently developing and characterizing preclinical mouse models that replicate cardiovascular toxicities linked to novel cancer immunotherapies, including immune checkpoint inhibitor-associated myocarditis.
Research Financial Analyst UCSF Medical CenterResearch Financial AnalystSan Francisco, CAInvolves activities associated with analyzing research funding trends and sources, forecasting, planning, and managing of research portfolios by performing some or all of the following: coordinating and identifying and developing and/or presenting proposals, contracts and other agreements; reviewing proposals to ensure institutional compliance and program success; negotiating, administering and monitoring contract and grant awards, including compliance with regulations, terms and conditions; financial management and reporting; and sub award/subcontract issuance and administration. Leads the organization, planning, establishment, and monitoring of fiscal budget control of contracts and grants administration, submissions, budgets, support documents, gifts, endowments, and privately funded projects for faculty research programs.
Clinical Data Associate Integrated Resources, IncClinical Data AssociateFoster City, CaliforniaContractorEssential Duties and Job Functions:Works collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists, Biomarker Statistical Programming group, Biomarker Biostatistics group, Biomarker Clinical Programming group, Bio banking and Sample Management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting. Clinical Data AssociateLead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experienceProject management experience of clinical trialsUnderstanding of clinical data management processesCommunication with cross-functional study team membersSpecific Responsibilities:This role will immediately assume biomarker data management responsibilities for representing biomarker data management at the biomarker Sub Team (BST) meetings.
Clinical Records Associate Integrated Resources, IncClinical Records AssociateFoster City, CaliforniaFull timePerform an inventory review for incoming CRO clinical study files; receive, index, and file preclinical study records; responsible for offsite archival of documents; participate in periodic file room utilization reviews; file incoming documents and retrieve documentation from the TMFR upon request. Job DescriptionJob Title: Clinical Records Associate - IILocation: Foster City, CADuration: 12 MonthsJob Description:Must meet all requirements for Clinical Records Assistant position and have demonstrated proficiency in all relevant areas.
Research Compliance Analyst UCSF Medical CenterResearch Compliance AnalystSan Francisco, CAAbility to use library software (EndNote) and University library resources to identify and catalog publications by Department faculty and trainees; ability to obtain publications in hard copy or. Ability to pay careful attention to detail to ensure accurate and complete maintenance of regulatory documents, through strict adherence to university, state, and federal guidelines, and GCP guidance.
Research Data Manager UCSF Medical CenterResearch Data ManagerSan Francisco, CAAs the coordinating center for the international Preclinical Design and Clinical Translation of Regimens for Tuberculosis (PReDiCTR-TB) Consortium, the laboratory integrates computational science, predictive modeling, translational pharmacology, clinical data, and quantitative decision science to support regimen selection, dose optimization, clinical trial design, and model-informed decision-making across the drug development lifecycle. The Savic Integrated Pharmacology Laboratory in the Department of Bioengineering and Therapeutic Sciences at the University of California, San Francisco (UCSF) is a global leader in model-informed drug development (MIDD) for infectious diseases and serves as an innovation hub for translational pharmacology, quantitative systems pharmacology (QSP), pharmacometrics, machine learning, artificial intelligence, and mechanistic modeling.