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 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.
NewResearch Associate 2, Critical Reagent Inventory Management (CRIM) BioMarin Pharmaceutical IncResearch Associate 2, Critical Reagent Inventory Management (CRIM)Novato, CA$77,600–$106,700 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 5 milesnttttttWithin 10 milesnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 500 milesttttttntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
Research Associate I/II Freenome IncResearch Associate I/IIBrisbane, CA$37.68–$46.69 / hourYou will work closely with multiple teams including molecular research, computational science, automation engineering, and clinical operations to develop the assays in a regulated, high-throughput environment as well as identify ways to rapidly iterate and improve on existing methods to evaluate technologies that can enhance our end-to-end test performance. Please note that individual total compensation for this position will be determined at the Company's sole discretion and may vary based on several factors, including but not limited to, location, skill level, years and depth of relevant experience, and education.
Clinical Laboratory Associate, Prenatal (Overnight Shift) BillionToOneClinical Laboratory Associate, Prenatal (Overnight Shift)Union City, CA$42.71–$61.50 / hourWe are looking for passionate Clinical Laboratory Associates (CLA) to be responsible for assisting our day-to-day operations, providing equipment maintenance in the clinical laboratory, completing the pre-analytical phase of testing (e.g., plasma and buffy coat isolation), performing quality assurance procedures, while complying with all local, state, and federal laboratory requirements. At 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.
Associate Director, Clinical Biomarker Development Revolution Medicines, Inc.Associate Director, Clinical Biomarker DevelopmentRedwood City, CA$186,000–$233,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. The Opportunity: The Associate Director in Clinical Biomarker Development team, within Translational Medicine will play a key role in the design, execution, and interpretation of clinical biomarker strategies across Revolution Medicine's oncology pipeline.
Associate Scientist, Oncology Research CytomX Therapeutics IncAssociate Scientist, Oncology ResearchSouth San Francisco, CA$115,000–$135,000 / yearHeadquarters Location: South San Francisco, CA, Company relocating to Emeryville, CA Fall of 2026. Associate Scientist, Oncology Research.
HTS Research Associate Octant BioHTS 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.
Associate Scientist, Oncology Research CytomX TherapeuticsAssociate Scientist, Oncology ResearchSouth San Francisco, CA$115,000–$135,000 / yearAs a bench scientist, the individual will design and conduct high quality experiments independently with guidance of the supervisor, and will be responsible for data analysis and interpretation, thorough and accurate documentation of work, as well as clear and transparent communication of results in group settings including internal and external project team meetings. As part of this commitment, we (and the agencies we work with) will assist individuals who have a disability with any reasonable accommodation requests related to employment, including completing the application process, interviewing, completing any pre-employment testing, participating in the employee selection process, and/or to perform essential job functions where the requested accommodation does not impose an undue hardship.
Clinical Research Coordinator (Phlebotomy) UCSF Medical CenterClinical Research Coordinator (Phlebotomy)San Francisco, CAThe Division of HIV, Infectious Diseases and Global Medicine at Zuckerberg San Francisco General Hospital (ZSFG) is an internationally recognized global leader in HIV clinical care, research and education and has grown to encompass a network of specialty clinics, multiple research and clinical trials, an HIV education program, an international research program in East Africa and a vibrant community forum for clinicians and researchers. Knowledgeable in phlebotomy issues, including performing phlebotomy, working knowledge of tubes and procedures required for blood draw of clinical laboratory tests, and sample processing for T-cell assays, flow cytometry, and other research assays; basic laboratory techniques (safe handling practices, preparing and labeling samples and reagents for studies, proper use, storage, and disposal of reagents).
Staff Research Associate III (Data Scientist) Veterans Health Research InstituteStaff Research Associate III (Data Scientist)San Francisco, CA$68,640–$93,060.24 / yearDesign and implement advanced machine learning models (e.g., deep learning, statistical modeling) to predict aortic disease risk progression. This role will be instrumental in leveraging big data approaches to analyze vast datasets, identify patterns, and develop predictive models.
Associate Director, Biostatistics Clinical Late Stage Revolution Medicines, Inc.Associate Director, Biostatistics Clinical Late StageRedwood City, CA$186,000–$233,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Assistant Clinical Research Coordinator UCSF Medical CenterAssistant Clinical Research CoordinatorSan Francisco, CAUnder the supervision and guidance of the Principal Investigator and Clinical Research Supervisor at the UCSF Memory and Aging Center, the Assistant Clinical Research Coordinator (ACRC) will serve as a liaison between research participants and other faculty/study staff members to perform entry-level duties related to the support and coordination of clinical studies in the UCSF Alzheimer's Disease Research Center and associated projects. The ACRC will coordinate the scheduling of study visit events such as neurological exams, nursing interviews, biospecimen collection, and will work to retain research participants though the end of their research participation.
NewAssociate Director, Clinical Operations Revolution Medicines, Inc.Associate Director, Clinical OperationsRedwood City, CA$186,000–$233,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Proven experience working with investigators, external experts and regulatory agencies and oversight of Contract Research Organizations and third-party vendors including realigning with CRO partners when deliverables are at risk, negotiating solutions and leading After Action Reviews to share lessons learned.
Clinical Data Associate - II Integrated Resources, IncClinical Data Associate - IIFoster City, CaliforniaContractorClinical Data Associate - IIWorks collaboratively with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting. Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery.
NewClinical Research Coordinator Phlebotomist UCSF Medical CenterClinical Research Coordinator PhlebotomistSan Francisco, CAActive protocols include PREVENT-LC (Early Antiviral Treatment to Prevent Viral Persistence and Inflammation as Drivers of Long COVID), PASC-RECOVER (Post-Acute Sequelae of SARS-CoV-2 Infection - Researching COVID to Enhance Recovery), and the LIINC cohort, and the CRC may be assigned to additional home- or clinic-based studies as the Division's research portfolio evolves. Job Summary: This position sits within the Division of HIV, Infectious Diseases and Global Medicine at Zuckerberg San Francisco General Hospital (ZSFG), and supports the LIINC (Long-term Impact of Infection with the Novel Coronavirus) and SCOPE (Study on the Consequences of the Protease Inhibitor Era) Research Programs, which conduct clinical and translational research on acute and post-acute infection syndromes related to COVID-19 and HIV.
Clinical Research Coordinator Rheumatology UCSF Medical CenterClinical Research Coordinator RheumatologySan 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, 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; manage Investigator's protocols in the Committee on Human Research 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; 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: Access, Stata, SASS/ SPSS, and Teleform programming platforms.
Clinical Research Coordinator (Osher Center) UCSF Medical CenterClinical Research Coordinator (Osher Center)San Francisco, CAThe employee's main responsibilities pertain to study implementation, including: implementing study protocols; modifying and managing IRB applications; managing databases and conducting data quality control; distributing survey materials on REDCap; recruiting, enrolling, and retaining study participants; conducting clinical interviews with research participants; conducting experimental tasks with mothers and children; recording study data in REDCap according to good clinical practice; building and/or modifying REDCap database and reports; tracking data collection; coordinating staff work schedules; assisting with training and oversight of other staff and volunteers; assuring compliance with all relevant regulatory agencies; overseeing study data integrity; reporting study progress to investigators; participating in any internal and external audits or reviews of study protocols; and performing other duties as assigned. 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 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.
Clinical Research Coordinator Nephrology UCSF Medical CenterClinical Research Coordinator NephrologySan Francisco, CAResponsibilities for all studies include: schedule patient visits and procedures; maintain accurate research charts and research study binders; perform accurate data collection and data entry; perform patient follow-up visits according to specific research study requirements; complete consent procedures and questionnaires with subjects; participate in research meetings; manage Investigator's protocols in the Committee on Human Research (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; and perform other duties as assigned. Also responsible for creating research accounts in Apex; linking patients to the research study and keeping their research status updated; linking encounters to the study and setting the research billing flag; creating lab orders and medication orders in Apex; scanning and uploading study consent forms into the patient's medical chart; reviewing lab results, current medications, radiology studies, and providers' progress notes for data collection into the research study database.
Staff Research Associate IV, Supervisor Veterans Health Research InstituteStaff Research Associate IV, SupervisorSan Francisco, CA$70,304–$120,016 / yearThe portfolio may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, large research grant awards, laboratory-based research, and/or programmatic clinical research activities, such as a clinical database and biorepository. 15% Exercises supervisory authority, including hiring, transferring, suspending, promoting, managing conduct and performance, discharging, assigning, rewarding, disciplining, and/or approving hours worked of at least 3 to 6 full-time equivalent (FTE) employees.
Clinical Research Coordinator Gastroenterology UCSF Medical CenterClinical Research Coordinator GastroenterologySan Francisco, CAIncumbent's duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies; 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, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investigator's protocols in the Committee on Human Research 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; 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: Access, Stata, SASS/ SPSS, and Teleform programming platforms.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorPalo Alto, CA$37–$45 / hourWe 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. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Research Associate 2 Natera IncResearch Associate 2San Carlos, CA$74,800–$93,500 / yearYou will execute Next-Generation Sequencing (NGS) workflows, cell-free DNA (cfDNA) extraction, and library preparation, generating the high-quality data required to advance our clinical diagnostic assays. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.
Associate Clinical Education Coordinator Guardant HealthAssociate Clinical Education CoordinatorRedwood City, California$67,300–$92,550 / yearAt least one year of Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred; Bachelor of Arts or Science in Clinical Science, Education, or related field preferred; Experience with Microsoft Office suite, and/or Smartsheets, and/or Salesforce for business use; Working knowledge of local, state, and federal laboratory regulations preferred; Able to integrate and apply feedback in a professional manner; Ability to work as part of a team; and. Hours and days may vary depending on operational needs; Standing or sitting for long periods of time may be necessary; May be exposed to hazardous materials, blood specimens and instruments with moving parts, heating or freezing elements and high-speed centrifugation; Manual and repetitive pipetting may be necessary; and.
Senior Research Associate Onyx BioSenior Research AssociateBerkeley, California$100,000–$130,000 / yearIn practice, you will work across our entire operation depending on need and priority: you’ll be supporting our sample collection kit/biobanking operations at times, and also running single-cell genomics and multiomics assays to support data generation at other times. You will work alongside two senior teammates—one leading R&D and assay development, the other leading platform/operations—providing the precise, reliable execution that turns precious patient samples into clean, reproducible multiomics data.
Sr. Clinical Development Engineer - Strategy Intuitive Surgical IncSr. Clinical Development Engineer - StrategySunnyvale, CACertain 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). U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.
Staff Research Associate I Veterans Health Research InstituteStaff Research Associate ISan Francisco, CA$24.11–$28.87 / hourPosition Definition: The Staff Research Associate I is responsible for participating in the day-to-day operations of routine, minimally complex clinical research programs and/or studies conducted by Principal Investigators (PIs) at the San Francisco VA. Assists with the development of data collection documents and instruments, maintains subject level documentation, and prepares documents, equipment and/or supplies identifies issues recommends solutions.
Senior Research Associate, DNA Encoded Library Technology ~ Contract Position Nurix Therapeutics, Inc.Senior Research Associate, DNA Encoded Library Technology ~ Contract PositionBrisbane, 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).
NewResearch Associate Belcan LLCResearch AssociateSouth San Francisco, CASupport in vivo scientists and collaborate with cross-functional teams to support preclinical oncology and pharmacology studies. or Associate Degree or GED with Certification with 5 years experience, in animal handing techniques, including tumor implantation, randomization, dosing IV and IP.
Operations Associate Alleviate HealthOperations AssociateSan Francisco, CaliforniaWe’ve now raised a $4.3M seed round led by a16z and are hiring a world-class team to solve the largest problem in drug development and win one of the largest opportunities in AI – while slashing the time it takes to bring life-changing medicines to the patients who desperately need them. To bring a life-saving medicine from the lab bench to patients, pharma companies spend tens of billions a year for research sites to qualify & screen hundreds of thousands of patients and then to stay in contact with those patients over years.
Staff Research Associate II, Supervisor Veterans Health Research InstituteStaff Research Associate II, SupervisorSan Francisco, CA$33–$48.68 / hourOverview: Oversee health services research project support, and manage grant, institutional and financial activities for Dr. Kelly's research focused on examining RSV vaccination risks and outcomes. Responsible for manuscript submissions, progress tracking and formulating response letters for revision to peer-reviewed journals and abstracts for scientific meetings for the PI, residents and fellows.
Clinical Laboratory Associate Guardant HealthClinical Laboratory AssociateRedwood City, California$38–$52 / hourAbility in giving and receiving constructive feedback, fostering open communication and continuous improvement; Demonstrates strong practical reasoning and sound judgment; Skilled in making informed and effective decisions; Exhibits attention to detail and a strong commitment to precision in all tasks; Strong computing skills; Knowledge of Good documentation practices; Working knowledge of reagent stability and storage, quality control policies, and factors that influence test results; Strong communicator with ability to maintain open communication with internal employees, managers; Able to integrate and apply feedback in a professional manner; and. Qualifications: Minimum of Associate degree or equivalent required; Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field preferred; Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred; Previous laboratory work experience preferred, with skills including (but not limited to) proper specimen collection or retrieval, patient preparation, labeling, handling, assay assist or assay preparation, preventive maintenance and troubleshooting, and/or transportation and storage of specimens.
Associate Director, Clinical Trial Management Annexon IncAssociate Director, Clinical Trial ManagementSan Francisco, CARemote$179,000–$200,000 / yearOur novel scientific approach targets upstream C1q to block the classical complement inflammatory cascade before it starts, and its therapeutic candidates are designed to provide meaningful benefits across multiple autoimmune, neurodegenerative and ophthalmic diseases. With proof-of concept data in Guillain-Barré syndrome, Huntington's disease and geographic atrophy, we are rigorously advancing our mid-to late-stage clinical trials to bring new potential treatments to patients as quickly as possible.
Process Engineering Associate I/II, Oncology BillionToOneProcess Engineering Associate I/II, OncologyMenlo Park, CA$75,029–$85,748 / yearThe PEA I is responsible for (1) developing new tools for improved clinical workflow efficiency, (2) analyzing process data to monitor and troubleshoot our high-throughput assays, 3) identifying root causes of recurring errors with proper documentation to enable long term corrective actions. At 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.
Research Associate, In Vivo RetroResearch Associate, In VivoRedwood City, CA$95,000–$115,000 / yearWe focus on cellular reprogramming and autophagy to rejuvenate cell and tissue function with the ultimate aim of adding 10 years to healthy human lifespan. In this role, you will: Perform dose administration (IP, SQ, RO, PO, IV), blood collection (RO, Cardiac, SM, tail vein), oral gavage administration, and necropsy in rodent models.
Associate Director, Clinical Business Operations Management Iovance Biotherapeutics IncAssociate Director, Clinical Business Operations ManagementSan Carlos, CARemote$175,000–$195,000 / yearMental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines. Supports the identification and prioritization of deliverables across clinical departments (i.e., Medical Writing, Biostatistics, Drug Safety, Clinical Science)., organizes cross-functional teams and tracks progress against goals and timelines.
Sr. Clinical Trial Associate ALX Oncology Inc.Sr. Clinical Trial AssociateSouth San Francisco, CA$100,000–$120,000A Clinical Trial Associate (CTA) supports clinical operations by supporting and progressively owning key study execution activities including startup,Trial Master Files (TMF) management, tracking study documents, assisting with site activation, and managing trial reports and supplies. Support Clinical Trial Manager (CTM), Study lead and Study Management Team (SMT) in study start up and executional activities.
Associate Director, Global Patient Safety Operations Revolution Medicines, Inc.Associate Director, Global Patient Safety OperationsRedwood City, CA$186,000–$233,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Associate Director, Clinical Development Mirum PharmaceuticalsAssociate Director, Clinical DevelopmentFoster City, CaliforniaThe Associate Director, Clinical Development will be responsible for supporting clinical trial related activities for Brelovitug, a key asset in Phase 3, on a cross-functional team of internal and external experts, investigators and government agencies. Activities include but are not limited to drafting key clinical trial and program-level documents, protocol development, support study startup, recruitment, ongoing clinical development management, and closeout as appropriate.
Clinical Project Manager Align TechnologyClinical Project ManagerSan Jose, California$129,300–$177,700 / yearSkills: o Ability to think critically and scientifically o Ability to give presentations and updates on clinical research/studies o Ability to write clinical reports and protocols o Ability to communicate effectively o Has a proactive mindset and strong drive to take initiative, actively seek opportunities and solutions o Has a go-getter attitude to take on challenges with determination and strives to deliver quality results Communication: Excellent presentation and communication skills. · Masters of Science preferred · 6-10 years’ experience in clinical research industry preferred · 2-5 years experience as Senior Clinical Research Associate · Dental industry experience preferred · Experience running clinical studies from a project management perspective required · Experience with SaMD clinical studies is preferred · Person must have familiarity with applicable FDA regulations .
Associate Director, Clinical Data Management Structure Therapeutics IncAssociate Director, Clinical Data ManagementSouth San Francisco, CA$180,000–$220,000 / yearThe companys 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. The AD serves as primary DM contact to collaborate closely with cross-functional teams, including Clinical Operations, Biostatistics, Clinical Development and Regulatory Affairs, to ensure that data management activities align with the overall clinical development strategy and regulatory requirements.
Associate Director, Regulatory Systems Revolution Medicines, Inc.Associate Director, Regulatory SystemsRedwood City, CA$186,000–$233,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. This individual will serve as the business owner for key regulatory systems and partner closely with Regulatory Affairs, Regulatory Operations, IT, Quality, Clinical, and external vendors to deliver scalable, compliant, and efficient business solutions.
Associate Director/Director, Clinical Product Development AccuScan SciencesAssociate Director/Director, Clinical Product DevelopmentMilpitas, CAThis position plays a critical leadership role in advancing molecular diagnostic products from LDT development through clinical validation, MolDx reimbursement, and potential IVD/CE-IVDR pathways, supporting multi-indication oncology programs. This role is responsible for translating scientific innovation into clinically validated, regulatory-ready, and commercially viable products, spanning assay development, clinical evidence generation, regulatory strategy, and market access.
Scientist II, mRNA Research & Production Profluent IncScientist II, mRNA Research & ProductionEmeryville, CA$147,000–$161,000 / yearLead and execute end-to-end research-grade automated mRNA production workflows, including template preparation, plasmid DNA sequencing data analysis, linearization, IVT, capping or cap analog workflows, nucleotide modification, purification, buffer exchange, storage, and batch release for research use. Use analytical platforms such as Fragment Analyzer, TapeStation, Bioanalyzer, gel or capillary electrophoresis, HPLC/UPLC, dsRNA ELISA, endotoxin assays, qPCR/ddPCR, and cell-based assays to characterize mRNA quality.
Postdoctoral Fellow - Next-Gen Sequencing Systems, Research & Early Development F. Hoffmann-La Roche LtdPostdoctoral Fellow - Next-Gen Sequencing Systems, Research & Early DevelopmentSanta Clara, CA$100,000–$106,000 / yearJoining our Systems Technology Group, you will play a major role in the Research and Early Development of new technology, devices, and instruments associated with our next-generation DNA sequencing and molecular diagnostic platforms. You will develop and implement microfabrication processes, including photolithography, etching, drilling, bonding, and dicing-and utilize precision metrology instruments to characterize components and evaluate manufacturing methodologies.
Associate Scientist, R&D Natera IncAssociate Scientist, R&DSan Carlos, CA$50–$57 / hourYou will engage deeply in the scientific process, conduct meticulous experiments, and collaborate closely with a cross-functional team of senior scientists, Lab operation, automation engineers, biostatisticians, and lab directors to advance cutting-edge technologies. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.
Associate Clinical Data Management Director Exelixis Inc.Associate Clinical Data Management DirectorAlameda, CA$163,000–$231,000 / yearEDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education/Experience: BS/BA degree in related discipline and a minimum of 11 years of related experience; or, MS/MA degree in related discipline and a minimum of 9 years of related experience; or, PhD in related discipline and a minimum of 5 years of related experience; or, Equivalent combination of education and experience. In collaboration with cross-functional teams, external partners, and support Data Managers, may serve as the lead study data manager for a large, complex trial or multiple, smaller studies.
NewDirector, Clinical Operations Jade BiosciencesDirector, Clinical OperationsSan Francisco, CaliforniaRemote$215,000–$240,000 / yearDirects the selection of CROs and other vendors (IxRS, Central Lab, ancillary/tech vendors), directs development of vendor Scopes of Work (SOW), scope changes, budgets, and vendor payments and partners with CROs and other vendors to deliver on study execution. The Director, Clinical Operations will oversee the strategic and operational execution of clinical trials, leading cross-functional teams and collaborating with internal stakeholders and external vendors.
Clinical Trial Manager CareDx IncClinical Trial ManagerBrisbane, CARemote$124,000–$155,000 / yearSpecific responsibilities include, but are not limited to: Lead the end-to-end execution of CareDx clinical trials, including but limited to site identification, study start-up, study conduct, monitoring and closeout, with full accountability of study timelines, budget and metrics; study submission to IRB/ECs; study document development and review (training documentation, ICF, study specific plans, eCRF Guidelines, lab test requisitions, etc.), plans and managing study-specific meetings (e.g. Provide cross-functional leadership across Clinical Operations, Data Management, Medical Affairs and other functional areas serving as the central point of coordination to ensure clear roles, accountability, and seamless clinical trial execution.
Associate Director, Biostatistics - Early Phase Revolution Medicines, Inc.Associate Director, Biostatistics - Early PhaseRedwood City, CA$186,000–$233,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.