NewLead Research Scientist Visa Technology and Operations LLCLead Research ScientistFoster City, CA$215,300–$344,600 / yearWe engage with the company's numerous technology and product teams, world-wide business partners, academics, and governments, to explore and develop technologies that will shape the future of the payments industry and impact the lives of billions of people. . Visa is a world leader in payments technology, facilitating transactions between consumers, merchants, financial institutions and government entities across more than 200 countries and territories, dedicated to uplifting everyone, everywhere by being the best way to pay and be paid.
NewStaff Research Scientist Visa Technology and Operations LLCStaff Research ScientistFoster City, CA$169,100–$270,800 / yearThe ideal candidate will focus on conducting advanced research in one or more subfields, for example, quantum error correction, quantum optimization, quantum simulation, quantum machine learning, distributed quantum computing and/or quantum security and privacy with the aim of applying their research outcomes to financial services and payments. We engage with the company's numerous technology and product teams, world-wide business partners, academics, and governments, to explore and develop technologies that will shape the future of the payments industry and impact the lives of billions of people.
NewCardio-Oncology & Heart Failure Cardiologist – Palo Alto, CA | Advanced Imaging & Research Program | Shareholder Track Palo Alto Foundation Medical GroupCardio-Oncology & Heart Failure Cardiologist – Palo Alto, CA | Advanced Imaging & Research Program | Shareholder TrackPalo Alto, CAOur current program has significant support with a dedicated program manager, experienced NPs, philanthropic funding, and Sutter Administration, with future goals of developing a robust data infrastructure for ongoing research endeavors including reduction of readmissions and telemedicine management. Candidate should have specific training in cardio-oncology (or at least 2 years of clinical work), ideally with leadership experience to further develop our current cardio-oncology program, and expertise in managing systolic and diastolic heart failure of various etiologies.
Staff Machine Learning Engineer (Research Scientist) - DFAI PlaidStaff Machine Learning Engineer (Research Scientist) - DFAISan Francisco, CA$249,120–$367,920 / yearPhD: 5–9+ years of industry experience with evidence of technical leadership (tech lead, principal/staff-equivalent roles) and end-to-end production ownership. We work with thousands of companies like Venmo, SoFi, several of the Fortune 500, and many of the largest banks to make it easy for people to connect their financial accounts to the apps and services they want to use.
NewResearch Chemist CalPortlandResearch ChemistJurupa Valley, CAStrong hands-on experience with testing methods and analytical techniques for cementitious materials, such as XRF, XRD, LOI, Blaine fineness, density, insoluble residue, free lime, ICP, isothermal calorimetry, and related procedures. The Research Chemist will independently execute laboratory testing and research activities using chemical, physical, and advanced instrumental techniques to support the analysis and characterization of cementitious materials.
Global Investment Research, Equity Research, Medical Technology & Healthcare IT, Associate The Goldman Sachs Group IncGlobal Investment Research, Equity Research, Medical Technology & Healthcare IT, AssociateSan Francisco, CA$150,000–$225,000 / yearOur analysts work on client-focused research in the equity, fixed-income, currency, and commodities markets, mining big data that enters markets around the world each day to identify game-changing insights. We''re committed to fostering and advancing diversity and inclusion in our own workplace and beyond by ensuring every individual within our firm has a number of opportunities to grow professionally and personally, from our training and development opportunities and firmwide networks to benefits, wellness and personal finance offerings and mindfulness programs.
Medical Affairs Research Manager Guardant Health IncMedical Affairs Research ManagerCARemote$164,900–$226,750 / yearThe Medical Research Manager will partner with multiple internal cross-functional stakeholders (Product, Technology Development and Bioinformatics, Clinical Development, Biostatistics, Managed Care and Reimbursement, Commercial) as well as external collaborators, advisors, and KOLs to identify clinical unmet need and evidence gaps to then lead the execution, and publication of clinical feasibility and validation studies, including those focused on clinical feasibility, clinical validity, and clinical utility. Primary Location: Remote - Open Position (USA) Primary Location Base Pay Range: $164,900 - $226,750 Other US Location(s) Base Pay Range: $164,900 - $226,750 If the role is performed in Colorado, the pay range for this job is: $164,900 - $226,750.
(Senior) Medical Science Liaison, External Research Tempus AI Inc(Senior) Medical Science Liaison, External ResearchCARemote$120,000–$190,000 / yearSupport the development and management of a Medical Research Strategy and Scientific Exchange Plans to guide the prioritization of new external research investments through conducting biannual clinical reviews of unmet needs for biomarkers for immunotherapy and targeted therapies, tumor response monitoring, and minimal residual disease in each cancer type. Engage academic KOLs and investigators in oncology to work on collaborative external research with Tempus, including investigator-initiated trials, assay grants for biobank samples or prospective trials, and real-world retrospective data studies.
Medical/Research Assistant National Institute of Clinical Research, Inc.Medical/Research AssistantHUNTINGTON BEACH, CANational Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a highly experienced Medical assistant with Phlebotomy experience to assist our research coordinators in clinical trials. The Research Assistant will be responsible for assisting the Research Study Coordinator in recruiting subjects for assigned clinical trials and coordinating the research activities and visits for the subjects enrolled in research projects.
Medical - Research Assistant National InstituteMedical - Research AssistantVictorville, CaliforniaThe Research Assistant will be responsible in assisting the Research Study Coordinator for recruiting subjects for assigned clinical trials, coordinate the research activities and visits for the subjects enrolled in research projects. Essentials functions include scheduling research visits for subject enrolled in clinical trials, performance of EKG, routine phlebotomy, other lab assessments such as vital signs, and obtaining necessary lab results for the subjects.
Clinical Research Coordinator I - Medical Group Cedars-Sinai Medical CenterClinical Research Coordinator I - Medical GroupLos Angeles, CAPrimary Duties & Responsibilities: Independent study coordination including assessing potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Medical Assistant - Clinical Research CenExelMedical Assistant - Clinical ResearchAnaheim, CaliforniaProvides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
Medical Assistant - Clinical Research (6:00 am - 6:00 pm) CenExelMedical Assistant - Clinical Research (6:00 am - 6:00 pm)Bellflower, CaliforniaPreparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Medical Assistant - Clinical Research Anaheim Clinical Trials, LLCMedical Assistant - Clinical ResearchAnaheim, CA$20–$21 / hourPart timeProvides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
Medical Assistant - Clinical Research (6:00 am - 6:00 pm) Clinical Innovation Inc.Medical Assistant - Clinical Research (6:00 am - 6:00 pm)Bellflower, CAPart timePreparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Clinical Research Assistant (Pre-Medical Track) Must Speak English and Spanish Angel City VAClinical Research Assistant (Pre-Medical Track) Must Speak English and SpanishLos Angeles, CaliforniaThe Clinical Research Assistant (CRA) is an entry-level, pre-professional role designed for pre-medical or health-sciences students seeking structured exposure to clinical research and patient-facing clinical environments. This role does not include independent study coordination or regulatory decision-making responsibilities and functions under close supervision at all times.
Clinical Research Coordinator I CAMRISClinical Research Coordinator ISan Diego, CAFull timeIn addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted. Manage and coordinate complex clinical trials: Handle complex logistics of trials, solve problems related to compliance or participant concerns, and make adjustments to protocols based on emerging situations during the study.
Staff Research Associate UCSF Medical CenterStaff Research AssociateSan Francisco, CAIn addition to the Moffitt-Long Hospital, very active units of the department exist at the Zuckerberg San Francisco General Hospital (ZSFG) (inpatient and outpatient, including an active trauma service); San Francisco Veterans Affairs Medical Center (inpatient and outpatient); Mount Zion Medical Center (outpatient, including 23 hour stays); Benioff Children''s Hospital Oakland; the UCSF Orthopedic Institute; the Benioff Children''s, Betty Irene Moore Women''s and Bakar Cancer (NIH-designated Cancer Center) Hospitals; and the Bayfront Medical Building (outpatient, Center for Pain Medicine) in the Mission Bay neighborhood. Under direct supervision with training provided, the position is assigned to assist in studying the pathogenesis of Cerebrovascular disease, including cell culture, maintaining genetically modified mouse lines, tissue section (frozen and paraffin), stains, and molecular assays (PCR, qPCR, protein assay).
Clinical Research Coordinator UCSF Medical CenterClinical Research CoordinatorSan Francisco, CAThe program requires 24/7 coverage of the autopsy pager, and the incumbent will share this on-call responsibility with the other members of the team and is contacted at the time of death to facilitate the procurement of donor tissue, frequently working with the Administrative Manager and Principal Investigator to problem-solve when unique autopsy situations arise (and occasionally addressing such situations independently.) Respond to inquiries from the public that come in through the autopsy cell phone line; evaluate eligibility for NDBB brain donation by checking LAVA and APEX; respond immediately (within 15 min) to death notifications and work with families, pathology team, funeral homes, and remote technicians/transport companies if applicable to ensure A. the timely procurement of tissue at death, B.
Postdoctoral Research Fellow Ellison Medical InstitutePostdoctoral Research FellowLos Angeles, CAFull timeFormerly known as the Ellison Institute of Technology Los Angeles, the Ellison Medical Institute strives to spark innovation, leverage technology, and drive interdisciplinary, patient-centered research to continually enhance health, reimagine and redefine cancer care, and transform lives. Advance Translational Immunology: Leverage expertise in immunology-particularly T cell activation and immune functional assays-to support the development of innovative biotechnology platforms with direct clinical and translational relevance.
Assistant Clinical Research Coordinator UCSF Medical CenterAssistant Clinical Research CoordinatorSan Francisco, CAMay be responsible for the coordination of one or more single or multi-site, active or follow-up clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical trial subjects; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments and assure collection and shipment of samples; assist research personnel to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and clean data into study databases, maintaining data quality; assist with data analysis; assist with preparation of reports and tables; attend team meetings; and perform other duties as assigned. Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: RedCap, Stata, and/or R programming platforms.
Research Protocol Analyst City of HopeResearch Protocol AnalystCAAs a successful candidate, you will: Protocol Management: Manage the full lifecycle of research protocol review-pre‑reviewing submissions, coordinating expert committee evaluations, preparing regulatory documentation, and ensuring timely, compliant investigator responses to achieve Protocol Review and Monitoring Committees (PRMCs), and Institutional Review Board (IRB) approval. Committee Meetings: Prepare complete meeting materials, provide regulatory guidance for complex submissions, and be fully knowledgeable about the ethical and regulatory requirements for conducting human subjects research to support and address committee questions during protocol reviews.
Clinical Research Coordinator (Spanish) UCSF Medical CenterClinical Research Coordinator (Spanish)San Francisco, CAKnowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
NewSpec 3, Clinical Research Kaygen Inc.Spec 3, Clinical ResearchIrvine, CA$40–$48 / hourTemporaryContractorFull timeReview clinical data for completeness across multiple research trials and conduct thorough documentation reviews for internal and external audits (e.g., FDA, TUV, PMDA) to ensure all essential Trial Master File (TMF) documents adhere to Good Documentation Practices, Edwards' internal SOPs, and relevant US and OUS regulations. Key Responsibilities: Participate in study start-up activities (e.g., tracking site readiness, communication with clinical trial sites about planning and logistics of site qualification visit and site initiation visit, and other associated supporting tasks), as well as study execution and closure activities.
NewClinical Research Specialist 3 Kaygen Inc.Clinical Research Specialist 3Irvine, CA$40–$48 / hourTemporaryContractorFull timeReview clinical data for completeness across multiple research trials and conduct thorough documentation reviews for internal and external audits (e.g., FDA, TUV, PMDA) to ensure all essential Trial Master File (TMF) documents adhere to Good Documentation Practices, Edwards' internal SOPs, and relevant US and OUS regulations. Participate in study start-up activities (e.g., tracking site readiness, communication with clinical trial sites about planning and logistics of site qualification visit and site initiation visit, and other associated supporting tasks), as well as study execution and closure activities.
Senior Director, Global Research Nursery Driscoll'sSenior Director, Global Research NurseryWatsonville, California$190,820–$262,380Provides leadership and development for regional nursery leaders, site managers, and technical teams while building organizational capabilities, both through formal as well as through informal relationships and organizational structures across the Enterprise. Responsibilities: Develops and implements Research Nursery strategies for all Global R&D breeding and research programs and is responsible for the execution of those strategies across a network of organizations and facilities, including some directly managed, as well as through internal and external partners and service providers.
Research Associate I- Alexanian Lab Gladstone Institute of Neurological DiseaseResearch Associate I- Alexanian LabSan Francisco, CA$28.35–$32.21 / hourComputational biology and AI: support analysis of large-scale genomic datasets, contribute to data processing and visualization, and participate in projects using machine learning models to understand cell states and predict gene regulatory programs. A 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.
Senior Clinical Research Coordinator Headlands Research IncSenior Clinical Research CoordinatorEscondido, CA$80,000–$90,000 / yearIf you're an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work-life balance, AMCR Institute may be the right next step in your career. Headlands Research AMCR Institute, located in Escondido, California, is dedicated to advancing metabolic and immunologic research through patient-centered, high-quality clinical trials.
Clinical Research Associate Veracyte IncClinical Research AssociateSouth San Francisco, CA$110,000–$127,000 / yearOur Veracyte Diagnostics Platform delivers high-performing cancer tests that are fueled by broad genomic and clinical data, deep bioinformatic and AI capabilities, and a powerful evidence-generation engine, which ultimately drives durable reimbursement and guideline inclusion for our tests, along with new insights to support continued innovation and pipeline development. Based at the San Francisco campus, the CRA partners with Clinical Affairs, R&D, Medical Affairs, and Laboratory Operations to ensure high-quality, compliant, and timely study execution.
Research Associate IV WerfenResearch Associate IVSan Diego, California$86,000–$110,000 / yearFull timeThe Research Associate IV contributes to the current and future Werfen Autoimmunity product lines by designing and performing a wide variety of laboratory techniques to assist in the development and transfer of new assays and/or improve on market assays. Education: Bachelor’s degree in related field (ex: Biology, Microbiology, Cellular Biology, Biochemistry) required plus at least 8+ years of experience working in a research and/or manufacturing lab required.
Clinical Research Coordinator Associate (2-Year Fixed Term) Stanford UniversityClinical Research Coordinator Associate (2-Year Fixed Term)Stanford, CA$34.56–$40.30 / hourThe Department of Psychiatry and Behavioral Sciences at Stanford Universitys School of Medicine is looking for an organized and motivated individual to fill the role of Clinical Research Coordinator Associate (CRCA) to coordinate aspects of a study focusing on fertility and family building in young adult female cancer survivors. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs.
Research Nurse - Part Time Apidel TechnologiesResearch Nurse - Part TimeStanford, CAContractorThe Research Nurse will lead the clinical components of participant visits, including obtaining vital signs; measuring height, weight, arm circumference, waist circumference, and hip circumference; performing 12-lead ECGs using sponsor-provided equipment; collecting blood, urine, and saliva specimens; conducting spirometry assessments; administering protocol-required medications, including albuterol (two puffs) via inhaler and valved holding chamber; and providing participant support and study-related refreshments as required by study protocols. Frequently stand/walk, sit, perform desk-based computer tasks, use a telephone, writing by hand, sort/file paperwork or parts, twist/bend/stoop/squat, and grasp lightly/fine manipulation.
Life Science Research Professional 1 (Fixed-Term: 2 Years/FTE: 50%) Stanford UniversityLife Science Research Professional 1 (Fixed-Term: 2 Years/FTE: 50%)Stanford, CA$32.58–$38.48 / hourThe pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs. PHYSICAL REQUIREMENTS*: Frequently stand, walk, twist, bend, stoop, squat, grasp lightly, use fine manipulation, grasp forcefully, perform desk-based computer tasks, use telephone, write by hand, lift, carry, and push and pull objects weighing over 40 pounds.
Clinical Research Coordinator II - IDCRP The Henry M Jackson Foundation for the Advancement of Military Medicine IncClinical Research Coordinator II - IDCRPSan Diego, CAWe serve military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. HJF is seeking a Clinical Research Coordinator II to perform clinical research and patient treatment in conjunction with one or more specified clinical research protocols.
Part-time Clinical Research Coordinator UCSF Medical CenterPart-time Clinical Research CoordinatorSan Francisco, CAStudies open to enrollment: Assist physicians in screening and checking eligibility for potential candidates for the clinical trials using APEX, clinical notes, and medical records; Initiates first contact with potential study candidate to introduce possible, appropriate clinical trial; Consents study participants; Registers participants to appropriate registration system; Maintains patient tracking forms, reporting and recording adverse events. Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.
Clinical Research Coordinator ECN Operating LLCClinical Research CoordinatorHuntington Beach, CAThe CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred , as this role may include specimen collection and basic clinical procedures.
NewResearch Associate University of Southern CaliforniaResearch AssociateLos Angeles, CaliforniaWe are seeking a highly motivated candidate with expertise in immunology, translational biology, organoid systems, and preferably computational analysis of large-scale datasets to join a multidisciplinary research program focused on clinically relevant liver disease. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate’s work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.“.
Regional Travel, Clinical Research Coordinator Care AccessRegional Travel, Clinical Research CoordinatorThousand Oaks, CARemote$75,000–$105,000 / yearWith programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
Senior Clinical Research Coordinator Headlands ResearchSenior Clinical Research CoordinatorEscondido, CaliforniaIf you’re an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work–life balance , AMCR Institute may be the right next step in your career. Headlands Research AMCR Institute, located in Escondido, California, is dedicated to advancing metabolic and immunologic research through patient-centered, high-quality clinical trials.
AI Research Scientist Intern GenMDAI Research Scientist InternPalo Alto, CaliforniaGenMD is just coming out of stealth, already revenue-generating, well-funded, and backed by premier investors with years of runway. The company was built out of years inside Stanford Medicine, working closely with world-class researchers and clinicians.
Research and Evaluation Manager Contra Costa CountyCAResearch and Evaluation ManagerContra Costa County, CA$126,439.90–$153,688.50 / yearIf you indicated that you possess experience in a research/evaluation position with responsibilities that included goal setting, program evaluation, survey design, statistical outcome reporting, report generation, and other complex administrative and budgetary analyses, how many years included lead or supervisory experience in directing, managing, and training staff on completing project tasks and deadlines?. We are looking for someone who: Possesses extensive leadership and management experience in supervising a team of dedicated Planner/Evaluators, Analysts or similar, with proven expertise in overseeing research and evaluation projects related to juvenile and criminal justice fields.
AVP, Alternatives Manager Research (Secondaries) Wilshire Advisors, LLCAVP, Alternatives Manager Research (Secondaries)Santa Monica, CA$110,000–$150,000 / yearDevelop and maintain deep relationships with private fund managers across the region, as well as create access to top-tier managers; proactively schedule and lead manager meetings and diligence calls (often high volume) to gather information and insights. Wilshire is seeking to recruit an investment professional to help lead research and due diligence efforts across all Alternatives segments with an emphasis on private markets (private equity, private credit, real assets) in North America.
Biomechanical Research and Testing Engineer II Alphatec SpineBiomechanical Research and Testing Engineer IICarlsbad, CAFor roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). Organize and analyze complex data sets, and contribute to the dissemination of scientific findings through presentation and writing for both internal and external audiences, including reports, conference abstracts, presentations, manuscripts, product collateral.
NewClinical Research Associate I City of HopeClinical Research Associate IDuarte, CACome join us as a Clinical Research Associate I in which you will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed, with mentorship by experienced staff. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.
Clinical Research Assistant I - Colorectal Cancer City of HopeClinical Research Assistant I - Colorectal CancerDuarte, CAJoin the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we''re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.
Quantum Topological Qubits Research Scientist GlobalFoundries IncQuantum Topological Qubits Research ScientistSanta Clara, CA$143,000–$275,000 / yearAs a PMTS, this role works closely with foundry customers to define the long-term technology architecture for topological qubit platforms while remaining actively engaged in experimental, modeling, and prototype activities. GlobalFoundries is a leading full-service semiconductor foundry providing a unique combination of design, development, and fabrication services to some of the world's most inspired technology companies.
Sr. Research Scientist Envista Holdings CorpSr. Research ScientistPomona, CA$156,100–$190,700 / yearEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.
Preclinical Veterinary Research Associate I, II, or III Pharmaron Beijing Co LtdPreclinical Veterinary Research Associate I, II, or IIISan Diego, CA$25–$35 / hourPharmaron San Diego is seeking a motivated Preclinical Veterinary Research Associate I, II, or III to join our Ophthalmology team supporting preclinical translational research programs focused on innovative ophthalmic therapeutics. This is an excellent opportunity for candidates with preclinical research, veterinary research, or in vivo laboratory experience who are looking to expand their technical skills and grow within a fast-paced and scientifically driven organization.
Research Associate I, II, III - Large Animal Pharmaron Beijing Co LtdResearch Associate I, II, III - Large AnimalCarlsbad, CA$25–$35 / hourFounded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. The successful candidate will work alongside experienced scientists, veterinarians, and study teams in a fast-paced CRO environment, contributing directly to translational research programs that help advance new technologies toward clinical development.
Clinical Research Coordinator Surgery UCSF Medical CenterClinical Research Coordinator SurgerySan Francisco, CAKnowledge of UCSF and departmental policies for dealing with research payments and reimbursements; patient safety and confidentiality; packing/shipping infectious substances; database building/analysis, and data management within some of the following platforms: Access, Stata, SASS/ SPSS, and Teleform. Experience applying the following regulations and guidelines:The Protection of Human Research SubjectsGood Clinical PracticeHealth Insurance Portability and Accountability Act (HIPAA)IRB regulationsSafe shipping practices (IATA)Environmental Health and Safety TrainingFire Safety Training.