Senior Manager, Clinical Quality Assurance Corcept Therapeutics IncSenior Manager, Clinical Quality AssuranceRedwood City, CA$173,430–$204,030 / yearSupport clinical study teams in risk management activities including the identification of critical to quality (CtQ) factors for each clinical study, implementing risk proportionate study activities in accordance with CtQs and the monitoring of identified risks to the CtQs. With 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.
Senior Clinical Trial Manager Sr CTM Corcept Therapeutics IncSenior Clinical Trial Manager Sr CTMRedwood City, CA$170,500–$200,700 / yearThis leader will work with cross-functional teams as well as vendors, clinical sites, and CROs to execute protocol requirements to ensure study deliverables, milestones, and objectives are met within timelines and budget. With 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.
NewClinical Research Associate AbbottClinical Research AssociateAlameda, California$73,900–$116,000 / yearGeneral Medical Devices: Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ngersticks. Demonstrate excellence in teamwork, solid interpersonal and communication skills including building rapport with team members/peers, study site staff, and clinical management.
Clinical Research Associate II Corcept TherapeuticsClinical Research Associate IIRedwood City, CA$129,400–$152,300 / 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 $129,400 - $152,300; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
NewClinical Data AMS Sr. Consultant DeloitteClinical Data AMS Sr. ConsultantSan Francisco, CA$120,200–$140,000 / yearThis role owns the health, stability, and compliance posture of a suite of clinical and regulatory R&D platforms - including Axway Secure Transport (ST), eClinical Elluminate, Eclipse (medical coding), and EAST - across the full engagement lifecycle: implementation, configuration, validation, and steady-state managed services. The team operates at the intersection of IT infrastructure, clinical operations, and quality/regulatory compliance, partnering closely with global business and technology stakeholders to support end-to-end clinical trial data lifecycles from data capture and coding through statistical analysis and submission-ready outputs.
IT Project Manager (Clinical Supply Chain) Iconma LLCIT Project Manager (Clinical Supply Chain)Foster City, CAScope Management: Manage the approved project scope, validate business and technical requirements, monitor scope changes, assess impacts, and ensure changes are reviewed and approved through the defined governance process. Requirement and Issue Tracking: Track business requirements, functional gaps, configuration decisions, defects, issues, and action items to closure using approved project management and delivery tools.
Manager, Clinical Supply Chain Revolution Medicines, Inc.Manager, Clinical Supply ChainRedwood City, CA$143,000–$178,000 / 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. Responsibilities: Serve as the clinical supply lead for assigned study(s) and develop/manage the clinical supply Develop and execute comprehensive clinical supply strategies for global clinical development programs from Phase I through Phase III, ensuring alignment with program objectives, enrollment assumptions, manufacturing timelines, and regulatory requirements.
Member of Technical Staff - Clinical AI Research Scientist Kinetic SystemsMember of Technical Staff - Clinical AI Research ScientistSan Francisco, CaliforniaYou'll help build novel datasets, environments, and benchmarks to identify capability gaps in current models, publish academic papers, and post-train models to push the SOTA while staying grounded to the demonstrated needs of our healthcare partners. Our mission is to advance the capabilities of frontier models for solving clinically and economically meaningful healthcare tasks.
Clinical Trials Manager Resources Connection IncClinical Trials ManagerSouth San Francisco, CAAs the Clinical Trials Manager, you will provide leadership to study teams, CROs, and vendors, oversee study budgets and forecasts, monitor trial spend against plans, and ensure effective financial stewardship of clinical programs. We've built a global network of over 2,600 experts across four regions, providing a comprehensive suite of solutions across on-demand talent, next-generation consulting, and outsourced services to support organizations at every stage of their growth journey.
Clinical Trial Manager (contract) ALX Oncology Holdings IncClinical Trial Manager (contract)South San Francisco, CAReporting to the Executive Director, Clinical Operations, the contract Clinical Trial Manager (CTM) will manage the day-to-day operational execution of global clinical trials from study start-up through closeout. ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives.
Head of Clinical Pharmacology Cytokinetics IncHead of Clinical PharmacologySouth San Francisco, CA$290,430–$357,000 / yearClinical Pharmacology Strategy • Develop and implement comprehensive clinical pharmacology strategies spanning FIH, SAD/MAD, food effect, drug-drug interaction (DDI), QT assessment, renal/hepatic impairment, intrinsic/extrinsic factor studies, and special populations. Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.
NewClinical Research Scientist - I (Neurology) Net2SourceClinical Research Scientist - I (Neurology)Foster City, CARemote$143.88–$179.86 / hourSupport the planning and execution of neurology clinical programs, including CIDP, through: Review of adjudication charters, endpoint assessment manuals, and related operational plans. Identification of clinical trial execution risks, operational gaps, and potential barriers to enrollment, data quality, and study delivery.
Clinical Trial Manager Revolution Medicines, Inc.Clinical Trial ManagerRedwood City, CA$120,000–$150,000 / 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: This is a unique opportunity for an experienced Clinical Operations Professional who has technical expertise in managing Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operations, Good Clinical Practice (GCP) and U.S. Food and Drug Administration (FDA) regulatory requirements.
Senior Director, Clinical Research Oncology Vir Biotechnology IncSenior Director, Clinical Research OncologySan Francisco, CA$235,500–$329,500 / yearOversee clinical science deliverables for assigned studies, including protocols and amendments, informed consent forms (ICFs), case report form (CRF) design and data review strategies, and clinical study reports (CSRs) as well as the clinical sections of regulatory submissions. This role requires an experienced MD, PhD or PharmD with deep expertise in oncology drug development and a proven track record of leading clinical research teams through complex development programs, from first‑in‑human through registration.
Director, Clinical Operations Maze Therapeutics IncDirector, Clinical OperationsSouth San Francisco, CA$232,000–$283,000 / yearServe as the operational Study Lead for a global pivotal Phase 3 study (North America, South America, Africa, and Europe), maintaining responsibility for successful execution from protocol development and start-up through enrollment, database lock, study closeout, submission support, and inspection readiness. Maintain a continuous state of inspection readiness across the study, including safety reporting, TMF completeness and quality, essential documentation, evidence of vendor oversight, issue and CAPA management, and audit preparedness, in close partnership with Quality Assurance (QA).
Clinical Trials Management Associate II Integrated Resources, IncClinical Trials Management Associate IIFoster City, CaliforniaContractorParticipates or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teams. With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required.
Clinical Trials Management Associate Integrated Resources, IncClinical Trials Management AssociateFoster City, CaliforniaContractorParticipates or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teams. With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required.
Clinical Scientist Corvus Pharmaceuticals IncClinical ScientistBurlingame, CA$130,000–$150,000 / yearAssist other team members in Clinical Development in the implementation and conduct of clinical trial which includes but not limited to review of enrollment packets, review of adverse events and all other clinical data generated during conduct of trial. Work closely with Data Management to ensure that all relevant clinical data is collected in a timely manner and assist with cleaning of data listings.
Clinical Research Coordinator (San Francisco) University of CaliforniaClinical Research Coordinator (San Francisco)San Francisco, CA$34.37–$55.27 / hourThe Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational level of the series to coordinate and execute research protocols, as directed by the Principal Investigator, Investigators, the Center Research Supervisor, and/or the Center Director; the incumbent may coordinate the data collection and operations of concurrent clinical research studies under the guidelines of research protocols and regulating agency policies. The study aims to improve mental health access and economic opportunity in the Mission District of San Francisco by expanding the community health workforce, strengthening cross-sector partnerships across health, social, and economic sectors, and addresses upstream structural factors such as housing instability, stigma, and fragmented care systems.
Associate Clinical SAS Programmer/Junior Statistician HeartFlowAssociate Clinical SAS Programmer/Junior StatisticianSan Francisco, CA$86,000–$112,000 / yearHeartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMapAnalysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). The Associate Clinical SAS Programmer/Junior Statistician plays a pivotal role in the clinical trial lifecycle by transforming raw clinical trial data into formatted, analysis-ready datasets and generating the outputs required for, conference, publication, and regulatory submissions.