Medical Director, Clinical Informatics, Emergency Medicine Sutter HealthMedical Director, Clinical Informatics, Emergency MedicineSan Francisco, CARecognized ability to energize, mobilize, influence, and build accountability with a broad range of stakeholders through effective communication of vision, and the fostering of productive and supportive working relationships with internal and external constituencies. Total compensation considers multiple factors, including, but not limited to a candidate's experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs.
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.
Open Source Research Software Engineer: Computational Infrastructure (0652) Job #87957 - Berkeley In University of CaliforniaOpen Source Research Software Engineer: Computational Infrastructure (0652) Job #87957 - Berkeley InBerkeley, CA$101,600–$189,800 / yearThese will include, but not be limited to, advances in core Jupyter components for collaboration and data sharing across deployments in separate hosting environments (ranging from local clusters and HPC facilities to the cloud), integration of AI agents and tools into the research workflow, sharing of intermediate results, code and pre-publication outputs with fine-grained access control, and fluid integration of these Jupyter deployments alongside existing research tools and environments that are independent of Jupyter. 5% Enables collaborators to design, implement, reproduce, and extend highly complex data analyses to address real-world research problems, including accessing data from varied multi-modal processing pipelines, working directly with domain scientists and open source communities as appropriate.
Elluminate Programmer / Clinical Data Programmer Perfict Global, Inc.Elluminate Programmer / Clinical Data ProgrammerConcord, CARemoteMinimum of 5 years SQL programming/clinical data programming/clinical data warehouse mapping experience in clinical trial conduct in a pharmaceutical company or contract research organization. Program and generate data review tools such as patient profiles and data listings in support of data review in Data Central and Clinical Data Analytics.
NewOpen Source Research Software Engineer: User Interfaces (0652) Job#88093 - BIDS University of CaliforniaOpen Source Research Software Engineer: User Interfaces (0652) Job#88093 - BIDSBerkeley, CA$101,600–$149,000 / yearThese will include, but not be limited to, advances in core Jupyter components for collaboration and data sharing across deployments in separate hosting environments (ranging from local clusters and HPC facilities to the cloud), integration of AI agents and tools into the research workflow, sharing of intermediate results, code and pre-publication outputs with fine-grained access control, and fluid integration of these Jupyter deployments alongside existing research tools and environments that are independent of Jupyter. Please submit a cover letter including 1) links to up to 3 publicly available GitHub repositories that highlight engagement in issues, pull requests, community discussions (or equivalent conversations on alternative git forge platforms), 2) links to up to 3 examples of code you have written to develop user interface software, and 3) a description of a previous role (paid or volunteer) where you have identified and delivered outcomes in the presence of uncertainty.
Sr. Associate, Clinical Supplies Planning and Logistics Structure Therapeutics IncSr. Associate, Clinical Supplies Planning and LogisticsSouth San Francisco, CA$109,000–$135,000 / yearCollaborate with external partners (CMOs, CROs, shipping and IRT vendors, study sites) and study team members to ensure successful execution of clinical trials Collaborate with Clinical Operations and Regulatory Affairs to provide packaging and labeling information, including labeling and packaging design in compliance with relevant SOPs, polices, and regulations Works closely with QA to ensure compliance with IP documentation, procedures, Lot numbers, managing expiration dates, and coordinating release schedules, Tracking GCP adherence at sites Participates in the review of IP-related study documents (e.g., pharmacy manual, IP section of protocol) and training materials for clinical study teams and investigational site use as needed. Job Responsibilities: As part of the Clinical Supplies Planning and Logistics team, participates in clinical supply and logistics activities, including but not limited to demand forecasting and supply planning, label text generation and approval, packaging and labeling operations at clinical supply vendors, batch record review, distribution management, temperature excursion, expiry extension, drug return and destruction records, and inventory management.
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 Medical Director, Early Clinical Development BioMarin Pharmaceutical IncSenior Medical Director, Early Clinical DevelopmentCA$284,000–$390,500 / yearntttttSearch JobsntttttntttttLocationntttttntttttSearch RadiusnttttttttttnttttttWithin 5 milesnttttttWithin 10 milesnttttttWithin 25 milesnttttttWithin 50 milesnttttttWithin 100 milesnttttttWithin 500 milesttttttntttttntttttntttttntttttntttt. nttttttDIN numbernttttttnttttttnttttttnttttt.
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 Scientist LatentResearch ScientistSan Francisco, California$225,000–$300,000 / yearYou will drive research from ambiguous problem definition through to validated results and downstream impact, shaping the technical direction of how models learn from longitudinal patient data. Our dataset represents one of the most clinically diverse populations in the United States, including patients with chronic illness and complex disease.
Sr. Clinical Trial Associate ALX Oncology Inc.Sr. Clinical Trial AssociateSouth San Francisco, CA$115,000–$125,000 / yearCTA) supports clinical trial execution from study start-up through close-out, with increasing ownership of activities including Trial Master File (TMF) management, site activation, study tracking, vendor coordination, and study documentation. Support oversight of CROs and other study vendors, including tracking deliverables, timelines, documentation, system access and assisting with review of vendor and study plans; proactively identify and address routine issues and escalate risks as appropriate.
Account Executive - Biotech, Business Development - Clinical Trials Division - San Fransico, CA Thermo Fisher Scientific IncAccount Executive - Biotech, Business Development - Clinical Trials Division - San Fransico, CASouth San Francisco, CA$103,600–$155,350 / yearNew Business Development including identifying new molecule opportunities with new or existing clients through understanding of the market, appointment based strategic selling, leveraging personal network, interaction with other Pharma Services Group (PSG), Clinical Research Group (CRG) and Thermo Fisher Scientific teams, and following up on leads. With more than 65 locations globally, we provide our clients with integrated, end-to-end capabilities through all phases of development, including API, biologics, viral vector services, formulation, clinical trial solutions, logistics services and commercial manufacturing.
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.
Sr. Clinical Trial Manager Structure Therapeutics IncSr. Clinical Trial ManagerSouth San Francisco, CA$171,000–$218,000 / yearIdentifies potential study issues/risks, escalates as needed and recommends/implements Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up. Minimum of 7+ years of related industry experience as a Clinical Research Associate or related function with increasing responsibility and scope Minimum of 3+ years study management experience in clinical and drug development Experience in selecting, managing, and overseeing sites, CROs, specialty labs and other service providers in global, multinational studies or programs.
AI Research Scientist Sprinter Health IncAI Research ScientistSan Francisco, CAYour work may include novel architectures, new training or evaluation techniques, long-horizon research bets, peer-reviewed validation studies, patents, and methods that ultimately graduate into production systems. Our team of clinicians, technologists, and operators have raised over $125M to date investors like a16z, General Catalyst, GV, and Accel and enjoy multi-year runway.
APP Manager, Inpatient and ORAC Stanford Health CareAPP Manager, Inpatient and ORACPALO ALTO, CA$106.01–$140.47 / hourThis role provides day-to-day operational leadership and management for APPs across the inpatient and ORAC service lines within Stanford Medicine Cancer Center and is responsible for APP hiring, onboarding, scheduling, performance management, regulatory support, and transition to practice coordination, while partnering with physician, nursing, and operational leaders to ensure effective staffing, workflow, workforce engagement, and support for key quality outcomes. Reporting to the APP Director, Inpatient & Oncology Rapid Assessment Clinic (ORAC) of the Cancer Destination Service Line (DSL), this is a unique opportunity at one of the most respected healthcare institutions in the U.S. This is an exceptional opportunity for an experienced APP leader to join one of the country''s top academic health systems focused on bridging a spirit of discovery with the very best in diagnosis and treatment, with outstanding quality, compassion, and coordination of care.
Research Assistant - 12 Month Fixed Term Stanford UniversityResearch Assistant - 12 Month Fixed TermStanford, CA$34.56–$40.30 / hourThe candidate should be comfortable in social settings interacting with patients in their hospital bed (at times in the same room for hours of testing), competent in using computers, basic knowledge in MATLAB (or equivalent) programming and have excellent interpersonal communication skills to support coordination among lab members, research personnel, collaborators, hospital staff, and patients. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs.
Staff, Product Development Lifecycle N-Power MedicineStaff, Product Development LifecycleRedwood City, California$192,165–$220,000 / yearThis individual will serve as the critical liaison between healthcare product management, operations, oncology data, and engineering - translating product requirements into engineering delivery, holding engineering accountable to the product roadmap, and ensuring that everything shipped meets the quality bar for a clinical-facing product. Minimum of 8 years of related experience with a Bachelor's degree; or 5 years and a Master's degree; or equivalent work experience, with seniority commensurate with a senior manager-level role with sound judgment operating independently and representing the function to leadership.
APP Manager, Cancer DSL Ambulatory Stanford Health CareAPP Manager, Cancer DSL AmbulatoryPALO ALTO, CA$106.01–$140.47 / hourThis role provides day-to-day operational leadership and management for APPs across the ambulatory service lines within Stanford Medicine Cancer Center and is responsible for APP hiring, onboarding, scheduling, performance management, regulatory support, and transition to practice coordination, while partnering with physician, nursing, and operational leaders to ensure effective staffing, workflow, workforce engagement, and support for key quality outcomes. Reporting to the APP Director, Ambulatory of the Cancer Destination Service Line (DSL), this is a unique opportunity at one of the most respected healthcare institutions in the U.S. This is an exceptional opportunity for an experienced APP leader to join one of the country''s top academic health systems focused on bridging a spirit of discovery with the very best in diagnosis and treatment, with outstanding quality, compassion, and coordination of care.
Clinical Trial Manager Sagimet Biosciences IncClinical Trial ManagerSan Mateo, CA$90–$100 / hourAdditional responsibilities include Independent oversight of outsourced clinical studies, protocol review for operational feasibility and consistency, CRO/vendor feasibility, request for proposal and bid defense process, country/site feasibility, tracking site selection, activation, and patient recruitment. Work with junior CTM for oversight of Trial Master Files (TMF) oversight plan and laisses with CRO for annual quality check; ensuring tracking of ICH-GCP and/or FDA CRF21 essential study documents.