20 Results for

Winter Research Jobs in San Jose, CA

Jobs

Newark, CA26 days ago

$99,000–$121,000 Per Year
Full-time

Responsibilities:Provide sponsor oversight of assigned investigative sites, serving as the primary operational and ensuring high – quality protocol execution, and compliance with GCP, and regulatory requirementsMonitor site performance through centralized and remote review of study data, key performance metrics, and monitoring outputs, including proactively identify and escalate issues with recommended mitigation strategiesSupport study start-up, conduct, and close-out activities, including site feasibility, activation, training, and close-out documentationEnsure timely collection, review, and maintenance of essential regulatory documents and maintain Trial Master File (TMF) completeness, quality and inspection readinessPartner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study’s risk-based monitoring strategyTrack and analyze protocol deviations, safety events, data discrepancies, and site performance trends; collaborate with cross-functional teams to drive timely resolutionSupport regulatory and inspection readiness by overseeing IRB/EC submissions and approvals, maintaining accurate site documentation, and contributing to audit and inspection preparation, responses, and follow-up activitiesCollaborate cross-functionally with Clinical Operations, Data Management, Safety, Regulatory Affairs, and Biostatistics, and support sponsor oversight of CROs and otherParticipate in investigator meetings, study team meetings, and internal governance as requiredQualifications:Bachelor’s degree in relevant scientific discipline with 2-5 years of experience in clinical research, clinical operations or healthcare-related roles or equivalent combination of education and experiencePrior experience as a Clinical Trial Assistant (CTA), Study Coordinator, or similar clinical research role requiredWorking knowledge of ICH-GCP, FDA regulations, and global clinical trial requirementsExperience with sponsor systems EDC, eTMF, CTMS and centralized monitoring toolsStrong analytical skills with the ability to interpret study and site-level performance trendsExcellent written and verbal communication skills with high level of attention to detailDemonstrated sponsor mindset with a focus on quality, accountability, and complianceAbility to work independently while escalating issues appropriatelyStrong problem abilities and proactive risk identification skillsEffective collaboration and stakeholder management abilitiesThrives in a collaborative environment and enjoys working cross-functionally to solve operational challenges. Building on prior experience in a Clinical Trial Assistant (CTA) or similar role, the CRA II independently manages assigned sites and supports study oversight of clinical trial execution.

Mountain View, CA30+ days ago

$118,000–$157,000 Per Year
Full-time
Employee

Note: By applying to this position you will have an opportunity to share your preferred working location from the following: Mountain View, CA, USA; Ann Arbor, MI, USA; Atlanta, GA, USA; Austin, TX, USA; Cambridge, MA, USA; Chicago, IL, USA; Irvine, CA, USA; Kirkland, WA, USA; Los Angeles, CA, USA; Madison, WI, USA; New York, NY, USA; Palo Alto, CA, USA; Pittsburgh, PA, USA; Goleta, CA, USA; San Bruno, CA, USA; Seattle, WA, USA; San Francisco, CA, USA; Sunnyvale, CA, USA; Washington D.C., DC, USA.Minimum qualifications: Currently enrolled in a PhD degree in Computer Science, Linguistics, Statistics, Biostatistics, Applied Mathematics, Operations Research, Economics, Natural Sciences, or related technical field. Whether we're shaping the future of sustainability, optimizing algorithms, or pioneering AI systems, our teams strive to continuously progress science, advance society, and improve the lives of billions of people.

Mountain View, CA30+ days ago

$98,000–$131,000 Per Year
Full-time
Employee

Note: By applying to this position you will have an opportunity to share your preferred working location from the following: Mountain View, CA, USA; Ann Arbor, MI, USA; Atlanta, GA, USA; Austin, TX, USA; Cambridge, MA, USA; Chicago, IL, USA; Irvine, CA, USA; Kirkland, WA, USA; Los Angeles, CA, USA; Madison, WI, USA; New York, NY, USA; Palo Alto, CA, USA; Pittsburgh, PA, USA; San Bruno, CA, USA; Seattle, WA, USA; San Francisco, CA, USA; Sunnyvale, CA, USA; Washington D.C., DC, USA; Princeton, NJ, USA.Minimum qualifications: Currently enrolled in a Bachelor's or Master’s degree in Computer Science, Linguistics, Statistics, Biostatistics, Applied Mathematics, Operations Research, Economics, Natural Sciences, or related technical field. Whether we're shaping the future of sustainability, optimizing algorithms, or pioneering AI systems, our teams strive to continuously progress science, advance society, and improve the lives of billions of people.

Palo Alto, CA20 days ago

Monitor recruitment of study subjects, data completion, and protocol deviations; Prepare regular progress reports on these matters and propose and implement strategies to keep team on target, with input from the principal investigator as needed; Schedule sessions, help with obtaining written informed consent, and run participants through their respective protocols; Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements; Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms; Conduct quality assessment of data in project redcap database. Coordinate community educational outreach events about dementia and aging in English and/or Spanish; Foster community relationships; Assist in creating outreach materials and utilize materials created by Principal Investigator (PI) and the team to conduct small educational events to increase dementia awareness in the community; Interview community participants to identify their educational needs; Assist the PI and the team to create educational materials based on community needs analyses.

Palo Alto, CA20 days ago

Palo Alto Veterans Institute for Research (PAVIR) is seeking a full-time Clinical Research Assistant to work under the guidance/direction of VAPAHCS Principal Investigator (PI) - Dr. Minal Vasanawala - while supporting different aspects of the clinical research program in Nuclear Medicine Service, which includes facilitating clinical trials from inception to closeout. PAVIR engages in the administration of funds and providing support for the conduct of research at the Veterans Affairs Palo Alto Health Care System (VAPAHCS) to find new and improved ways to combat human disease and help people with disabilities.

Palo Alto, CA20 days ago

Assist with identification, screening, and enrollment of study subjects; Communicate with subjects about study procedures and obtain informed consent; Coordinate with study team and subjects to schedule visits and conduct follow-ups; Administer questionnaires and assessment instruments to subjects; Collaborate with study team to ensure that protocols are followed completely, labs are ordered and reviewed as required, and that all elements of patient safety and protection are present; Oversee data collection and data reconciliation; check data for completeness and verify as needed; Prepare treatment room for participants, including setting up video and audio recordings of sessions. Required: Bachelor's degree or equivalent experience required; Valid Driver's License; 2+ years of relevant clinical research experience (can include undergraduate); Desired: 3 years or more of relevant clinical research experience; Clinical research experience in including subject recruitment and screening; Prior experience in a mental health setting.

Sunnyvale, CA7 days ago

Assist with the development and management of study electronic clinical trial master file (eTMF) and maintain study documentation and clinical trial management system (e.g., correspondence, CRFs, study approval documents), trip reports, site contact documentation, monthly status reports (e.g., enrollment, adverse events, budget, etc.). Co-Management of site start-up/activation process, including heavy contribution to the preparation of study-related documents and complete checklists, able to help with clinical trial agreements and budget negotiation, finalization of clinical monitoring plan, training materials, etc.

West Menlo Park, CA30+ days ago

Required: Bachelor's degree or equivalent experience; At least 1 year of relevant research experience (can be undergraduate experience); Preferred: Master's degree; Previous experience working in the VA system and/or experience with intervention trials in oncology, subject recruitment and screening; Understanding of statistics and familiarity with STATA or similar data analysis software; Strong interpersonal skills. With assistance from the PI, Dr. Manali Patel, the Research Assistant will perform data collection, data entry, data management, simple data analysis, and creation of reports for funders as well as peer reviewed publications.

Stanford, CA30+ days ago

Contractor

Formally supervise, train, and/or mentor new staff or students, as assigned, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and performing related duties, in addition to instruction on project work. Working conditions: Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.

Milpitas, CA30+ days ago

You 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.

Redwood City, CA30+ days ago

Blackstone Talent Group is a wholly owned subsidiary of Blackstone Technology Group, a global IT services and software firm that implements technological solutions across commercial industry verticals and the US Federal Government. Our enzymes can drive improvements, such as higher yields, reduced energy usage and waste generation, improve efficiency in manufacturing and greater sensitivity in genomic and diagnostic applications.

Foster City, CA30+ days ago

$71,485–$89,356 Per Year

dosing routes (IV, IP, PO, subcutaneous), in-life and terminal blood collection, tumor inoculation, and handling of tissues during necropsy and processing for ex vivo analysis. therapeutics in pre-clinical models and will be responsible for daily in vivo study execution, data .

Menlo Park, California30+ days ago

$33.75–$41.25 Per Hour

or M.S./M.A. in Science, Engineering, or a related field such as Computer Science, Physics, Statistics, Applied Mathematics, Mechanical Engineering, Electrical Engineering, Applied Physics, Chemistry, Cognitive Science or Biomedical Engineering or related field. For over five decades, we've connected the lessons of past failures with tomorrow's solutions to advise clients as they innovate technologically complex products and processes, ensure the safety and health of their users, and address the challenges of sustainability.

Foster City, CA7 days ago

Senior Research Associate in the Biologics Pivotal & Commercial Cell Culture Process Development function will execute cell culture process laboratory experiments for biologics entities during pivotal development (phases II/III, commercial). Hands-on laboratory operations experience including shake flask, high-throughput bioreactor, bench scale bioreactor, and pilot scale cultures.

Menlo Park, California7 days ago

$55,580–$70,304 Per Year

Overview: SRI Biosciences Division is looking for a highly motivated Research Associate (RA) to contribute to multiple innovative programs spanning from drug target discovery to cell and gene therapies and drug delivery. For appointment as a Research Associate IINew grad Masters degree in Cell Biology, Molecular Biology, Biotechnology, Bioengineering, Neuroscience or related field or a Bachelors degree with at least 3 years of experience.

Foster City, CA30+ days ago

Primary responsibilities will include: designing, validating and performing Client cell-based immunology and virology assays;evaluating new targets and therapeutic approaches for curing HIV;supporting in vivo proof-of-concept studies in models of chronic HIV infection;understanding properties of the latent HIV reservoir in experimental models and clinical settings;interpreting results, and proactively troubleshooting technical challenges. The ideal candidate will have hands-on experience in one or more of the following techniques: immune cell functional assays, multi-color flow cytometry, primary cell isolation and culture, ELISA/Luminex, molecular biology techniques such as RNA/DNA isolation, qPCR, cloning and virus production.

South San Francisco, CA30+ days ago

$78,391–$98,005 Per Year

Experience with immortalized and/or primary cell culture, cell viability assessment, Luminex/ELISAs, gene expression analysis, high content screening, confocal microscopy, and flow cytometry is highly desired. ✅ Bachelors (BS/BA) in pharmacology, pharmaceutical science, biology, bioengineering, chemistry, physiology, or related discipline is required; Masters (MS) degree is desirable but not required.

Foster City, CA30+ days ago

$88,291–$110,364 Per Year

We are seeking to hire a Senior Research Associate, Drug Metabolism in Foster City, CA. · BS/MS degree in biology, chemistry, pharmacology, or related life science discipline with 2+ .

South San Francisco, CA30+ days ago

$68,174–$85,222 Per Year

Culturing mammalian cells for viral production in shake flasks, spinner flasks, spin tubes, deep well . · This includes small scale (shaker flasks, spinner flasks, spin tubes, deep well) and/or benchtop .

Newark, CA26 days ago

$136,000–$160,000 Per Year
Full-time

Proven problem-solving skills and tools, and ability to manage complex operational issues in a fast paced environmentExperience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,)Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences as requiredRemote work considered; preference for candidates able to attend the office weekly (Newark or Waltham)The anticipated annualized base pay range for this full-time position is $136,000-$160,000. Position Summary (Hybrid Location): The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of clinical trials, from study planning through close-out and reporting.

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Winter Research Jobs in San Jose, CA

Jobs

In House Clinical Research AssociateArdelyx

Student Researcher, PhD, Winter/Summer 2026Google

Student Researcher, BS/MS, Winter/Summer 2026Google

Clinical Research Assistant – Dementia and AgingPAVIR

Clinical Research Assistant – Nuclear Medicine ServicePAVIR

Clinical Research Assistant – Exploratory Therapeutics LaboratoryPAVIR

Senior Clinical Research AssociateIconma

Clinical Research Assistant – Health EducatorPAVIR

Clinical Research Coordinator 2Apidel Technologies

Research AssociateAccuraGen

Analytical Development Research AssociateBlackstone Talent Group

In Vivo Research AssociateTap Growth ai

Research AssistantExponent Inc.

Research Associate - IIIMACDILLIONS GLOBAL ENERGY

Bioscience Research AssociateSRI International

Research Associate - Biology - IILancesoft

Research Associate IIITap Growth ai

Senior Research Associate, Drug MetabolismTap Growth ai

Cell Line Development Research AssociateTap Growth ai

Clinical Trial ManagerArdelyx

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