Life Sciences Research Associate – Regenerative Medicine PAVIRLife Sciences Research Associate – Regenerative MedicinePalo Alto, CAFull timeStrong scientific writing skills and demonstrated capacity to drive first author publications;Knowledge of safe handling/storage of biohazardous chemicals & bloodborne pathogens;Solid training in general lab skills such as micro-pipetting, PCR analysis, cell culture, immunofluorescence staining, and biomaterials characterization;Solid training in analytical skills, including routine calculations of dilution factors and solution concentrations as well as using Excel and other programs for data calculation and analysis or biostatistical analysis;Knowledge of research procedures and protocols gained through education or experience;Experience in a variety of research techniques/methods and follow-up data collection;Knowledge of laboratory safety rules and procedures;Excellent communication skills (written and verbal), including public speaking skills;Ability to work independently and proactively;Ability to work within a team context and collaborate with other lab personnel. on the design and execution of laboratory experiments; Serve as the main contact for experiments;Develop and validate experimental protocols;Analyze data from experiments; Prepare charts for presentations and publication;Write papers on projects for publication;Perform general lab organization; Guide and train lab technicians or other lab members;Other research activities as assigned.
Research Scientist, Life Sciences AnthropicResearch Scientist, Life SciencesSan Francisco, CA$300,000–$320,000 / yearThis research continues many of the directions our team worked on prior to Anthropic, including: GPT-3, Circuit-Based Interpretability, Multimodal Neurons, Scaling Laws, AI & Compute, Concrete Problems in AI Safety, and Learning from Human Preferences. Build and ship agentic tools and integrations that let Claude execute real life science workflows - bioinformatics pipelines, database queries, analysis notebooks, literature review.
Associate Medical Director, Oncology Corcept TherapeuticsAssociate Medical Director, OncologyRedwood City, CA$229,300–$269,800 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. The pay range that the Company reasonably expects to pay for this headquarters-based position is $229,300-$269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Director, Clinical Trial Finance Structure Therapeutics IncDirector, Clinical Trial FinanceSouth San Francisco, CA$205,000–$250,000 / yearThe 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. Drive financial planning, budgeting, forecasting, and long-range planning for clinical trials; oversee financial management across programs, including accruals and variance analysis, in alignment with corporate objectives.
Gladstone Infectious Disease Institute/Ucsf Department Of Bioengineering And Therapeutics Sciences - Faculty Position Gladstone InstitutesGladstone Infectious Disease Institute/Ucsf Department Of Bioengineering And Therapeutics Sciences - Faculty PositionSan Francisco, CA$150,000–$350,000 / yearOur nimble structure and proximity to a world-renowned clinical and research university and to the San Francisco Bay Area biotechnology hub make for a uniquely exciting and supportive environment for investigators interested in taking risks and in building wide collaboration networks. Gladstone investigators direct world-class research programs that span neurological and cardiovascular diseases, cancer, immunology, virology and bioinformatics, all united by a common desire to overcome unsolved diseases through transformative biomedical research.
Disease-focused Neuroscience and Translational Neurobiology Faculty Position | Gladstone Institutes and UCSF Gladstone InstitutesDisease-focused Neuroscience and Translational Neurobiology Faculty Position | Gladstone Institutes and UCSFSan Francisco, CaliforniaA 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.
Gladstone Infectious Disease Institute/UCSF Department of Bioengineering and Therapeutics Sciences - Faculty Position Gladstone InstitutesGladstone Infectious Disease Institute/UCSF Department of Bioengineering and Therapeutics Sciences - Faculty PositionSan Francisco, CaliforniaOur nimble structure and proximity to a world-renowned clinical and research university and to the San Francisco Bay Area biotechnology hub make for a uniquely exciting and supportive environment for investigators interested in taking risks and in building wide collaboration networks. Gladstone investigators direct world-class research programs that span neurological and cardiovascular diseases, cancer, immunology, virology and bioinformatics, all united by a common desire to overcome unsolved diseases through transformative biomedical research.
Staff Software Engineer – Data Team #4555 GRAILStaff Software Engineer – Data Team #4555Menlo Park, CAThis is a software engineering role focused on building complex production-grade systems that work with data in dynamic, regulated environments as opposed to assembling off-the-shelf ETL tools or writing SQL heavy pipelines, This position offers significant autonomy and scope for impact. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine’s greatest challenges.
Sr. 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.
FSP - QC Reviewer Thermo Fisher ScientificFSP - QC ReviewerFoster City, CaliforniaWithin 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.
GCP Audit Support Actalent IncGCP Audit SupportAlameda, CARemote$55–$60 / hourThe ideal candidate will possess hands-on experience with Veeva Quality Vault, a strong understanding of GCP/GVP regulations, and experience supporting clinical quality auditing programs. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Quality Compliance Manager Actalent IncQuality Compliance ManagerAlameda, CARemote$55–$60 / hourThe ideal candidate will possess hands-on experience with Veeva Quality Vault, a strong understanding of GCP/GVP regulations, and experience supporting clinical quality auditing programs. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
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.
On-site Clinical Research Associate Protagonist Therapeutics IncOn-site Clinical Research AssociateNewark, CA$125,000–$135,000 / yearThe Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs. Serves as the internal primary site operations lead, working with the Project Manager and CROs to achieve efficient study set-up and initiation, ongoing data monitoring all the way through successful study execution and site close-out.
NewSr. Clinical Research Associate Intuitive Surgical IncSr. Clinical Research AssociateSunnyvale, CAAssist 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.
Clinical Research Coordinator - Pediatrics Research UCSF Medical CenterClinical Research Coordinator - Pediatrics ResearchSan Francisco, CAThe CRC's duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investigator's protocols in the Institutional Review Board (IRB) online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols. The Clinical Research Coordinator (CRC) 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) in the Department of Pediatrics; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Senior Clinical Research Associate Corcept TherapeuticsSenior Clinical Research AssociateRedwood City, CA$149,000–$170,000 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. The pay range that the Company reasonably expects to pay for this headquarters-based position is $149,000-$170,000; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
NewSr. Clinical Research Coordinator - Division of HIV (Part-Time) UCSF Medical CenterSr. Clinical Research Coordinator - Division of HIV (Part-Time)San Francisco, CAIn addition to leadership role for the CalCURE study, this position will support research efforts in the SF IDRC to include coordinating efforts for such sponsors as the Advancing Clinical Trials Globally (ACTG) a Division of AIDS (DAIDS) network, the Division of Microbiology and Infectious Disease (DMID) network and industry-sponsors such as Gilead, Glaxo Smith Kline, and Merck. The Sr CRC will serve as the primary study coordinator and program manager, overseeing conduct of the study at all participating sites, including study coordination, staff training, protocol and study material development, regulatory oversight, and coordination with the study team leadership, study sites, data manager, statistician and the IRB.
Clinical Trials Research Coordinator I Artech LLCClinical Trials Research Coordinator ISan Jose, CA$30–$32 / hourAdditionally, the role involves supporting the development and implementation of routine quality control and assurance measures and providing feedback to research staff and management as instructed. Associate’s degree in Science, Public Health, Health Care Administration, or a directly related field OR a minimum of one (1) year of experience in clinical research or a directly related field.
Clinical Research Coordinator, HF StratAcuity Staffing Partners IncClinical Research Coordinator, HFBurlingame, CA$50–$55 / hourThey will be comfortable collaborating with research scientists, engineers, designers, product teams, legal partners, vendors, and external collaborators to ensure successful study execution and generation of high-quality data that informs both scientific research and product development. Bachelors degree or higher in Human Factors, Human-Computer Interaction (HCI), Psychology, Cognitive Science, Public Health, Biomedical Engineering, Life Sciences, Clinical Research, or a related field involving human subjects research.