Associate Director, Clinical Operations Structure Therapeutics IncAssociate Director, Clinical OperationsSouth San Francisco, CA$186,000–$220,000 / yearCross-Functional Collaboration: Work closely with Preclinical, Biostatistics, Data Management, Clinical Supplies, Safety/PV, and Medical Affairs teams to ensure seamless study execution and IMP accountability, including sample management and study plan reviews. 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.
Sr. Clinical Trial Assistant Actalent IncSr. Clinical Trial AssistantSouth San Francisco, CARemote$50–$60 / hourIf 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. 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.
Clinical Trial Assistant Actalent IncClinical Trial AssistantSouth San Francisco, CARemote$50–$60 / hourIf 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. 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.
Clinical Trial Assistant Intuitive Surgical IncClinical Trial AssistantSunnyvale, CA$70,000–$94,800 / yearEstablish, organize and maintain trial master file and clinical trial management system to ensure regulatory and protocol compliance including maintenance of study essential documentation (e.g., correspondence, CRFs, study approval documents, curriculum vita, etc…), trip reports, site contact documentation, monthly status reports (e.g., enrollment, adverse events, budget, etc.). 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.
Associate Director/Director, Clinical Science Lycia TherapeuticsAssociate Director/Director, Clinical ScienceSouth San Francisco, CA$190,000–$225,000 / yearResponsible for development of study protocols, case report forms (CRFs), consent forms, investigators brochure, development of charters (e.g., Independent Data Monitoring Committee, Safety Monitoring Committee) and other essential trial documents. This position is responsible for driving clinical development activities, ensuring scientific integrity, and collaborating with cross-functional teams to advance innovative therapies through all stages of clinical development.
Senior Clinical Study Manager Intuitive Surgical IncSenior Clinical Study ManagerSunnyvale, CAAccountable for the planning and execution of the clinical studies including site selection, review of potential patient recruitment and projections, creation of study related documents (protocols, case report forms, Informed consents, Clinical trial agreements, study reports), organizing IRB/EC submissions with follow-thorough to ensure successful progress. As a member of the Clinical Affairs team, this role will be accountable for working with key stakeholders to design and develop clinical protocols and other key study documents, effectively interact with key opinion leaders (KOLs) and execute clinical studies (pre-market or post-market studies), independently and with minimal supervision.
Assistant, Associate, or full Professor: Stanford-Surgery Policy Improvement Research & Education (S-SPIRE) Center stanfordAssistant, Associate, or full Professor: Stanford-Surgery Policy Improvement Research & Education (S-SPIRE) CenterPalo Alto, CaliforniaThe Stanford-Surgery Policy Improvement Research & Education (S-SPIRE) Center in the Department of Surgery at Stanford University seeks a candidate with expertise in developing and implementing research initiatives that leverage AI techniques to enhance surgical decision-making, improve patient outcomes, and/or advance translational surgical research to join the Department as Assistant Professor, Associate Professor, or Professor in the University Medical Line (UML), University Tenure Line (UTL), Non-Tenure Line (Research) (NTL-R). The major criteria for appointment for faculty in the University Medical Line (UML) shall be excellence in the overall mix of clinical care, clinical teaching, scholarly activity that advances clinical medicine, and institutional service appropriate to the programmatic need the individual is expected to fulfill.
NewLife Sciences Research Associate II - Regenerative Medicine PAVIRLife Sciences Research Associate II - Regenerative MedicinePalo Alto, CAFull timeQUALIFICATIONS Required: PhDAt least three years of prior research experience in biology, bioengineering, cell biology, molecular biology or a related discipline (can include during studies);Advanced knowledge of scientific research methodology;Ability to troubleshoot an experiment as necessary;Exquisite record keeping and experimental documentation capabilities;Excellent organizational skills;Strong 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, genomic and plasmid DNA preparation, protein measurements, and tissue homogenization;Solid training in biomaterials fabrication and characterizationSolid 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;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.
NewLife 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.
NewResearch Associate - Biology - III LanceSoft IncResearch Associate - Biology - IIIFoster City, CA$50 / hourwill be highly proficient in murine handling techniques including various dosing routes (IV, IP, PO, subcutaneous), in-life and terminal blood collection, and handling of tissues during. " Proficiency with various mouse handling techniques including dosing (PO, IV, SQ, IP), body weight measurements, in life and terminal blood collection, and collection and.
Sr. Clinical Study Manager Intuitive Surgical IncSr. Clinical Study ManagerSunnyvale, CAAccountable for the planning and execution of the clinical studies including site selection, review of potential patient recruitment and projections, creation of study related documents (protocols, case report forms, Informed consents, Clinical trial agreements, study reports), organizing IRB/EC submissions with follow-thorough to ensure successful progress. The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, develop clinical study reports, or help the development of clinical publications.
NewSenior Research Associate FreenomeSenior Research AssociateBrisbane, CA$97,850–$126,000 / yearCollaborate with Quality Control Lab, Manufacturing lab, Quality, and Regulatory to transfer reagent quality control methods and manufacturing processes from Development to Operations and support the implementation of the methods and processes in Operations. You will work closely with Scientists, Automation Engineers, and Computational Biologists to develop, optimize, and characterize efficient automated workflows to improve experimental and clinical throughput in a regulated high throughput environment.
Senior Research Associate, HPC Production (Fixed-Term Contract) Arc InstituteSenior Research Associate, HPC Production (Fixed-Term Contract)Palo Alto, CA$84,250–$114,250 / yearIn this role, you will serve as a dedicated producer of hematopoietic progenitor cells (HPCs), differentiating both parental and genetically edited human stem cells to supply high-quality HPCs for downstream research across multiple Tech Center teams. You will routinely execute staggered weekly rounds of HPC production, working ahead of demand by coordinating with requesting teams, scaling each round to meet projected needs, and maintaining the reagent and consumable stocks required to keep production uninterrupted.
Senior Research Associate, NGS - Genomics Platform (Fixed-Term Contract) Arc InstituteSenior Research Associate, NGS - Genomics Platform (Fixed-Term Contract)Palo Alto, CA$84,250–$114,250 / yearYou will work closely with scientists across Arc to coordinate sequencing submissions, perform sequencing operations, ensure rigorous quality control, and help maintain efficient, reliable production workflows across multiple next-generation sequencing platforms. Our two Institute Initiatives reflect this model in action: Virtual Cell Initiative : Building a full-stack virtual cell model to identify disease mechanisms and nominate drug targets, accelerating the path from biological insight to clinical trials.
Senior Research Associate (Contractor) FreenomeSenior Research Associate (Contractor)Brisbane, CAYou will work cross-functionally with Research & Development teams, automation and process engineering, computational science, and clinical operations to develop and transfer NGS-based assays in a regulated, high-throughput environment. Build productive working relationships and collaborate with engineers and clinical laboratory members to transition development protocols into clinical production, including automation, validation experiments, and SOP development.
Director, Clinical AI Technologies Structure Therapeutics IncDirector, Clinical AI TechnologiesSouth San Francisco, CA$237,000–$285,000 / 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. Position Summary: The Director of Clinical AI Technologies is responsible for translating clinical operation needs into AI-driven solutions to lead the strategy, implementation, and scaling of artificial intelligence (AI) solutions that enhance the execution and performance of clinical trials.
Associate Scientist, Research Laboratory Operations Revolution MedicinesAssociate Scientist, Research Laboratory OperationsRedwood City, California$119,000–$149,000 / 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. Proficiency with various mouse handling techniques including dosing (IV, PO, SC, IP), tumor inoculation/measurements, in life and terminal blood collection, survival surgeries, and handling of tissues during necropsy and processing for ex vivo analysis.
NewResearch Associate, ADCs Ridge Biotechnologies, Inc.Research Associate, ADCsSan Carlos, CAUsing our powerful experimental and computational platform built on large datasets generated by cell-free synthesis, biorthogonal chemistries, and ever-improving machine learning models, Ridge is pioneering the design of new medicines and scalable production methods that enable our partners to bring life-saving therapies to patients in need. In recent months, we've secured multiple partnerships and launched our first product lines: NativeLink enzymes that provide precise and stable bioconjugation without modification of protein sequence, glycan, or disulfide bonds; ProTrigger protease-cleavable linkers that enable selective drug release in the tumor microenvironment; and novel enzyme-based Catalytic Medicines.
Associate Scientist, Research Laboratory Operations Revolution Medicines IncAssociate Scientist, Research Laboratory OperationsRedwood City, CA$119,000–$149,000 / 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. Proficiency with various mouse handling techniques including dosing (IV, PO, SC, IP), tumor inoculation/measurements, in life and terminal blood collection, survival surgeries, and handling of tissues during necropsy and processing for ex vivo analysis.
Senior Research Associate KariusSenior Research AssociateRedwood City, CABy unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide. The company’s platform is already delivering unprecedented insights into the microbial landscape, providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood, and helping industry accelerate the development of therapeutic solutions.