35 Results for

Winter Research Jobs in San Francisco, CA

Jobs

Stanford, CA16 days ago

$40–$50 Per Hour
Temporary
Contractor

Manage research project databases, develop flow sheets and other study-related documents, and complete study documents/case report forms. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.

South San Francisco, CA26 days ago

$27.01–$32 Per Hour
Full-time
Employee

Responsibilities include characterization of synthetic molecule drug substance, including small molecules, peptides and oligonucleotides, and delivery systems, method development, execution of analytical methods, and new technology evaluation. The successful candidate will accomplish our mission through innovation and teamwork, creative problem-solving, and use of state-of-the-art technology including UHPLC-MS, multidimensional HPLC, GC, KF, UV, and CAD.

Newark, CA30+ 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

$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.

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.

San Francisco, California30+ days ago

Remote

Responsibilities : Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol; Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and. Qualifications : Must have a minimum of a Bachelor’s degree in a health or science related field; Experience as a Clinical Research Coordinator (minimum 1 year); Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely; Must maintain a valid driver’s license and the ability to drive to monitoring sites; Proficient knowledge of Microsoft® Office; Strong communication and presentation skills; and.

Palo Alto, CA30+ 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, CA30+ 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.

Walnut Creek, CA15 days ago

Full-time

Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of oncology, cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.

Palo Alto, CA30+ 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.

Stanford, CA15 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. Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

Stanford, CA15 days ago

Contractor

Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.

Santa Clara, CA16 days ago

We operate with a purpose-driven, agile, and collaborative culture, where each team member plays a meaningful role in advancing solutions that improve patient outcomes. As our clinical program grows, we are building a dedicated clinical operations team to support early feasibility studies and future pivotal trials.

Foster City, CA30+ days ago

Contractor

Primary responsibilities will include: designing, validating and performing novel 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. PHD will be Overqualified The ideal candidate must 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.

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.

Walnut Creek, CA8 days ago

Full-time

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Stocks lab supplies - unloads and organizes lab supplies in on-site lab supply storage room; maintains an inventory of lab supplies and re-orders when needed; assists in purchasing new equipment and supplies as needed.

Novato, CA30+ days ago

$40–$47 Per Hour

Bachelor’s Degree in Chemistry, Biochemistry, Analytical Chemistry, Chemical Engineering or related field with 6+ years of relevant experience, OR Master’s Degree with 4+ years of relevant experience. • Support the Separations and Biophysical Assays team within the Analytical Sciences group in method development and routine testing for biologics such as proteins, peptides, and conjugates.

Palo Alto, CA8 days ago

Prepares consolidated reports (e.g., monthly status/recruitment/quality metric reports, annual continuing reviews, responding to data queries, payment reimbursement accounting, protocol deviation, resolve tracking log discrepancies, personnel training adherence, etc.) for management, Sponsor, and higher echelon review. The CRC is responsible for participant recruitment/enrollment, coordination of study activities, data collection, analysis of data and project activities, documentation of activities, meeting reporting requirements, and providing oversight to study activities under the site Pl's authority.

Richmond, CA21 days ago

Outstanding customer service; Great verbal communication and writing skills; Meticulous attention to detail; Computer skills including web research and email skills; Ability to multi task and be flexible in the midst of changing priorities; Able to take both initiative and direction comfortably; Exceptional telephone skills; Customer focused, warm and engaging personality; Great listening skills; Strong problem solving skills; Professional presence; comfortable interacting with all customers and vendors; Consistent and reliable work ethic – integrity is critical; Ability to operate computer and other equipment in the office. We are a rapidly growing Aerospace Hardware distribution company in the Pt Richmond vicinity seeking an articulate, friendly, detail-oriented, smart and energetic person to assist with general office duties, communicating with customers and vendors, as well as keeping us organized.

Berkeley, CA30+ days ago

$70,000–$95,000

Fraudulent emails claiming to be sent by Azalea or Azalea employees may come from similar sounding emails with endings like “@azaleajobs.com” or “@azalea.com” or even emails ending in common public domain addresses with endings like “@gmail.com,” There can also be instances of fraudulent communication that use the names and pictures of known company employees claiming to be sent from those employees, or that even link out to fake websites that were created to look and feel like the real company website.

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.

Walnut Creek, CA30+ days ago

Full-time

The Flourish Research Walnut Creek site, formerly known as Diablo Clinical Research in Walnut Creek, has proudly served the East Bay community for 30 years as a dedicated clinical research facility conducting Phase 1–3 trials with major pharmaceutical sponsors and biotech innovators. Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines.

Foster City, CA9 days ago

$45–$50 Per Hour

Our group is highly collaborative, and we support all Client research and exploratory projects across several therapeutic areas including virology, inflammation, oncology, and respiratory disease. The role also entails working in a Biological Safety cabinet to reformat individual samples into appropriate labware for long term storage.

Palo Alto, CA25 days ago

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. The Clinical Research Data Analyst will directly support a busy and high-performing research program by working both independently and as part of a team on clinical data analysis.

Vallejo, California16 days ago

The position requires teaching using a comprehensive range of didactic methods—including lectures, labs, ultrasound, and procedures—across a full broad spectrum of system topics, learner mentorship, precepting, exam proctoring, fostering interdisciplinary research, and participating in academic and service responsibilities at the College and University. In addition to the College of Osteopathic Medicine, Touro University’s campus includes the College of Pharmacy, and the College of Education and Health Sciences, which includes graduate-level programs in education, nursing, Physician Assistant, and Masters in Public Health.

South San Francisco, CA15 days ago

$78,000–$95,000 Per Year

As a Clinical Trial Assistant (CTA), you will assist the clinical research teams in clinical trial conduct, oversight, and logistics by providing administration and project tracking support. Ensures study documents filed into the Veeva Vault electronic Trial Master File comply with filing guidelines and acceptability criteria.

Vallejo, California30+ days ago

$105,000–$140,000 Per Year

TUC is committed to being an institution that not only serves the variety of learners we teach and the patient populations we serve, but also pursues proficiency and mastery in community building, learner-centered instruction, and innovative teaching and learning that inform academic excellence. The successful candidate will have the opportunity to develop a research or scholarship program in their own biological field and/or in medical education while working with a talented team of departmental instructors in new state-of-the-art educational facilities.

New!

San Francisco, CA6 days ago

$130,200–$393,200 Per Year

The Division of Otology/Neurotology is renowned for cochlear implant research, work in central auditory processing, and other clinically relevant research, including outcomes research. Within the clinical realm, the Division has robust clinical volume in chronic ear surgery, vestibular pathology, and skull base tumor work in partnership with the renowned neurosurgery department at UCSF.

Vallejo, California30+ days ago

Touro University California (TUC) is a private, nonprofit institution committed to educating caring professionals in the fields of osteopathic medicine, pharmacy, public health, nursing, education, and physician assistant studies. This faculty member will contribute to the delivery of our integrated, systems-based curriculum for osteopathic medical students (COM) and postbaccalaureate students in the Master of Science in Medical Health Sciences (MSMHS) program.

Vallejo, California30+ days ago

Touro University California (TUC) is a private, nonprofit institution committed to educating caring professionals in the fields of osteopathic medicine, pharmacy, public health, nursing, education, and physician assistant studies. These faculty will contribute to an integrated, systems-based medical curriculum for osteopathic medical students (COM) and postbaccalaureate students in the Master of Science in Medical Health Sciences (MSMHS) program.

Oakland, CA30+ days ago

Our cutting-edge Heart and Vascular program provides not only basic preventative and general cardiology care but also sub specialized care including complex coronary interventions, structural heart and valvular procedures, electrophysiology, comprehensive cardiac imaging, advanced heart failure, cardio-oncology, women s health, and clinical research. Community Information:Oakland's landscape is a picturesque mix of lovely hillside neighborhoods; exciting and diverse architecture; a bustling waterfront; two shimmering lakes; 19 miles of shoreline along the San Francisco Bay; unparalleled Bay views; and more parks and open space per capita than any other city in the Bay Area.

New!

San Francisco, CA3 days ago

$84,552–$105,720 Per Year

Misconduct Disclosure Requirement: As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct, are currently being investigated for misconduct, left a position during an investigation for alleged misconduct, or have filed an appeal with a previous employer. The Associate will contribute to ongoing experiment-driven development efforts and participate in forward-looking R&D projects targeting future upgrades such as the High-Luminosity Large Hadron Collider and next-generation computing architectures.

South San Francisco, CA30+ days ago

$156,000–$195,000

As an Associate Director, the candidate is expected to represent translational sciences as a translational medicine lead for clinical studies and work closely with the clinical development team members including bioanalysis, clinical operations, regulatory affairs, quality, medical writing, safety, clinical research and clinical leadership. As part of the collaborative research team role, the candidate is expected to work with individuals across research and translational research groups, including discovery research, drug development and protein sciences, preclinical bioanalysis and other junior staff within translational research organization.

South San Francisco, California30+ days ago

Employee

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Winter Research Jobs in San Francisco, CA

Clinical Research Coordinator(Oncology) Collabera

Research Associate I Talent Software Services

In House Clinical Research Associate Ardelyx

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

Student Researcher, PhD, Winter/Summer 2026 Google

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) Medpace, Inc.

Clinical Research Assistant – Dementia and Aging PAVIR

Clinical Research Assistant – Nuclear Medicine Service PAVIR

Clinical Research Assistant Flourish Research

Clinical Research Assistant – Exploratory Therapeutics Laboratory PAVIR

Clinical Research Coordinator 2 Apidel Technologies

Clinical Research Coordinator Apidel Technologies

Clinical Research Associate - VahatiCor T45 Labs

Research Associate - Biology - II Integrated Resources, Inc

Research Associate AccuraGen

Laboratory Technician - Clinical Research Flourish Research

Sr Research Associate II Joulé

Clinical Research Coordinator – Cooperative Studies Program PAVIR

Sales / Research Associate / Admin Aerotech Solutions Inc

Research Associate I/II, Viral Vector Production Azalea Therapeutics, Inc.

Research Assistant Exponent Inc.

Clinical Research Coordinator Flourish Research

Research Associate – Biologics Inventory – Discovery Sciences & Technologies Iconma

Clinical Research Data Analyst II – Chronic Liver Diseases PAVIR

DO/MD Faculty Position: Assistant/Associate Professor, Clinical Sciences & Community Health - College of Osteopathic Medicine Touro University California

Clinical Trial Assistant Rigel Pharmaceuticals, Inc.

Assistant or Associate Professor - Anatomy Touro University California

Instructor/Assistant/Associate/Full Level Professor in Otology/Neurotology University of California , San Francisco

Pathology Assistant or Associate Professor, Foundational Biomedical Sciences Touro University California

Assistant or Associate Professor, Foundational Biomedical Sciences (Pathology and/or Microbiology) Touro University California

Nurse Practitioner/Physician Assistant, Cardiology - Oakland/Castro Valley, CA Sutter Health

Scientific Engineering Associate Lawrence Berkeley Lab

Associate Director, Translational Science Star Therapeutics

Strategy Insights & Planning Associate Consultant - Clinical Trials Risk-Based Quality Management (RBQM) ZS

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