Senior Clinical Scientist Intuitive Surgical IncSenior Clinical ScientistSunnyvale, CAThe purpose of this job is to work collaboratively to develop strategies for the creation of CEPs followed by the development of clinical evaluation reports (CERs) per EU MDR, to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, re-certification and proposed indication/labeling changes. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).
Senior Talent Acquisition Specialist Novotech Health Holdings Pte LtdSenior Talent Acquisition SpecialistSouth San Francisco, CA$110,000–$145,000 / yearThe ideal candidate will have a strong track record of recruiting for clinical research and clinical operations roles, including positions such as Clinical Research Associates (CRAs), Clinical Trial Managers, Clinical Project Managers, Clinical Research Coordinators, Regulatory Affairs professionals, Medical Monitors, Data Managers, Biostatisticians, and other clinical development professionals. By offering trust, flexibility, and autonomy through programs like NovoLife, our flexible benefits framework, we empower team members to create an effective work-life balance that delivers professional satisfaction and maximum results for clients.
CRC Melanoma and Cutaneous Oncology UCSF Medical CenterCRC Melanoma and Cutaneous OncologySan Francisco, CAIncumbent's duties may include, but will not be limited to, supporting the management and coordinating the tasks of single or multiple clinical research studies; managing and updating databases to ensure data integrity; acting as intermediary between sponsors, research staff, and various UCSF departments; help assure compliance with all relevant regulatory agencies; maintaining relevant regulatory documents in partnership with the Regulatory department; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; and performing 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: Access, Stata, SASS/ SPSS, and Teleform programming platforms.
CLIN RSCH SUPV 1 UCSF Medical CenterCLIN RSCH SUPV 1San Francisco, CAIn addition, the Division has significant and complex financial and administrative relationships with the Department of Medicine and the UCSF Medical Center, as well as large patient care programs in the sections noted above, large clinical, federal, and privately supported research programs, and six faculty laboratories. Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goals.
Protocol Project Manager UCSF Medical CenterProtocol Project ManagerSan Francisco, CAEnsure timely processing of new protocols through the activation pipeline including Medicare coverage analysis and budget sign off, informed consent approval and IRB submission, contract execution, and billing set up; prepare reports and trackers to keep the Disease Site Committee appraised of activation status for all new protocols. Forward all investigator-initiated modification requests to the protocol editors in a timely manner, and send all protocol amendments from industry sponsors to the regulatory affairs specialists, ITR Clinical Trials Budget Office and post-award analysts.
Associate Director, Quality SonoThera IncAssociate Director, QualitySouth San Francisco, CA$80–$93 / hourThis salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location. The successful candidate will establish quality frameworks from the ground up and lead quality initiatives that support the company''s pipeline from preclinical research through clinical development in a fast-paced, resource-conscious environment.
Director, Scientific Affairs Mirum Pharmaceuticals IncDirector, Scientific AffairsFoster City, CARemoteIdentifies, can gain access to, and develops professional relationships with thought leaders and other healthcare professionals, active and potential study investigators, and professional organizations within their assigned geography. Utilizes scientific resources to deliver impactful presentations to varying audiences and in a variety of different settings including (but not limited to) advisory boards and patient advocacy groups.
Clinical Research Associate Contractor Freenome IncClinical Research Associate ContractorCARemoteYou are passionate about clinical research, attention to detail and Good Clinical Practice, and you will have a significant impact on the continued growth of an organization dedicated to changing the entire landscape of cancer. Write and submit reports of investigational site findings and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate.
Senior Manager, Communications, Corporate Communications-Research Communications Kaiser PermanenteSenior Manager, Communications, Corporate Communications-Research CommunicationsPleasanton, CAManages designated units by translating business plans into tactical action items; communicating goals and objectives; ensuring all policies and procedures are followed; overseeing the completion of work assignments; assuming responsibility for decision making; aligning team efforts; building accountability for and measuring progress in achieving results; incorporating resources, costs, and forecasts into unit plans; removing obstacles that impact performance; guiding performance and developing contingency plans accordingly; partnering with key stakeholders and business leaders to ensure products and/or services meet requirements and expectations while aligning with departmental strategies; and influencing units to operate in alignment with business objectives. Manages the development of strategic communication plans by consulting with clients and stakeholders to identify business objectives, key performance indicators, and communication requirements; gathering and analyzing data and information; obtaining input and resources to fulfill communication plan objectives; ensuring plans are aligned with the organizational strategy; managing project schedules; providing input into and managing budgets and resources; identifying and leveraging appropriate audiences and channels; influencing stakeholders on strategic direction; and providing strategic support on a variety of organizational initiatives.
Equity Research Associate - Biotechnology Jefferies Financial Group IncEquity Research Associate - BiotechnologySan Francisco, CA$100,000–$120,000 / yearJefferies is a leading global, full-service investment banking and capital markets firm that provides advisory, sales and trading, research, and wealth and asset management services. Prior to Jefferies, he gained equity research experience in the biotechnology and software sectors at Wells Fargo, RBC Capital Markets, and Wedbush Securities.
Research Associate, Biobanking Parallel BioResearch Associate, BiobankingSan Francisco, CaliforniaAbility to pass respirator fit testing and comply with PPE requirements (per OSHA 29 CFR 1910.134), including maintaining facial hair compliant with a proper respirator seal. Receive, log, and process human biological samples (e.g., whole blood, buffy coats, lymphoid tissues) following established biosafety and ethical guidelines.
Research Associate BillionToOneResearch AssociateMenlo Park, CA$75,029–$85,748 / yearAt BillionToOne, we've built a category-defining, publicly traded company on Nasdaq where transparency fuels trust, collaboration drives breakthroughs, and every contribution moves the needle on our mission to make life-changing diagnostics accessible to all. You will have the chance to use cutting-edge molecular techniques, next-generation sequencing, and robotic tools to move assays from research prototypes to analyzing thousands of real patient samples in our clinical lab as a commercially available product.
Associate Clinical Trials Administrator Procept BioroboticsAssociate Clinical Trials AdministratorSan Jose, CAIt continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept's history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do.
Senior Research Associate, DNA Encoded Library Technology Nurix Therapeutics, Inc.Senior Research Associate, DNA Encoded Library TechnologyBrisbane, CA$101,690–$116,226 / yearWe are seeking a talented and motivated chemist to join our Discovery Chemistry team and contribute to the design and synthesis of DNA-encoded libraries (DELs). B.S. or higher in Chemistry, Biochemistry, or Medicinal Chemistry with 5 years of industrial experience (title determined by experience).
Principal Mechanical Engineer, Next-Gen Sequencing Systems, Research & Early Development F. Hoffmann-La Roche LtdPrincipal Mechanical Engineer, Next-Gen Sequencing Systems, Research & Early DevelopmentSanta Clara, CA$110,400–$205,400 / yearFrom robust sample isolation and preparation tools to novel sequencing technology and advanced bioinformatics, we are developing differentiated, highly integrated end-to-end solutions for next-generation sequencing, resulting in a sample in, result out workflow. You have demonstrated hands-on experience designing, developing, and testing complex electro-mechanical, pneumatic, thermal, or fluidic assemblies, preferably for life science or diagnostic instrumentation.
Senior Mechanical Engineer, Research & Early Development F. Hoffmann-La Roche LtdSenior Mechanical Engineer, Research & Early DevelopmentSanta Clara, CA$87,500–$162,500 / yearYou have a Bachelor''s in Mechanical Engineering (or a closely related discipline), with 4+ years of relevant industry experience; or a Master''s in Mechanical Engineering (or a closely related discipline), with 2+ years of relevant industry experience; or a PhD in in Mechanical Engineering (or a closely related discipline), with 1+ years of relevant industry experience. From robust sample isolation and preparation tools to novel sequencing technology and advanced bioinformatics, we are developing differentiated, highly integrated end-to-end solutions for next-generation sequencing, resulting in a sample in, result out workflow.
NewPrincipal Automation Research Engineer, Next Gen Sequencing Systems F. Hoffmann-La Roche LtdPrincipal Automation Research Engineer, Next Gen Sequencing SystemsSanta Clara, CA$110,600–$205,500 / yearWe are seeking a highly collaborative Principal Automation Research Engineer to contribute to the research and development of current and future automated platforms, while simultaneously building the tools to democratize key processes and eliminate bottlenecks. From robust sample isolation and preparation tools to novel sequencing technology and advanced bioinformatics, we are developing differentiated, highly integrated end-to-end solutions for next-generation sequencing workflows.
HTS Research Associate Octant IncHTS Research AssociateEmeryville, CA$75,000–$93,000 / yearThe Navigator is an expanding set of drug discovery and development capabilities with three interwoven components that operate together: Generative Biology - Multiplexed measurements from engineered sensors in human cells to understand cellular mechanisms. You bring strong technical skills in high-throughput plate-based assays, laboratory automation, and quantitative data analysis, along with excellent communication and an ability to thrive in a dynamic, fast-paced environment.
Research Technician AlljoinedResearch TechnicianSan Francisco, CaliforniaYou will work hands-on with EEG hardware and experimental workflows, sitting at the intersection of human interaction and high-throughput data collection - directly enabling the neural decoding breakthroughs our team is pursuing. We apply deep learning research to large scale EEG datasets to decode multimedia input, eventually moving to internal thought.
Senior Staff Clinical Quality Associate (Onsite) Stryker CorpSenior Staff Clinical Quality Associate (Onsite)Fremont, CA$115,600–$192,600 / yearHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. This role provides quality and compliance oversight for clinical research activities, ensuring processes, documentation, systems, and vendor operations remain compliant, inspection-ready, and aligned with global regulatory and quality requirements.