Sr. Clinical Trial Associate ALX Oncology Holdings IncSr. 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.
Clinical Research Assistant – Health Educator PAVIRClinical Research Assistant – Health EducatorMenlo Park, CATemporaryQUALIFICATIONS:Required: Bachelor's degree or equivalent experience;At least 1 year of relevant research experience (can be undergraduate experience);Preferred: Master's degree; Previous experience working in the VA system and/or experience with intervention trials in oncology, subject recruitment and screening;Understanding of statistics and familiarity with STATA or similar data analysis software;Strong interpersonal skills. With assistance from the PI, Dr. Manali Patel, the Health Educator will perform data collection, data entry, data management, simple data analysis, and creation of reports for funders as well as peer reviewed publications.
Clinical Trial Manager CTM Corcept Therapeutics IncClinical Trial Manager CTMRedwood City, CA$156,600–$184,300 / 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. Manages, either directly or through supervised delegation, other study-wide activities such as external vendors, sample handling, drug re-supply, investigator payments, overall data quality, and overall central records quality.
Clinical Research Engineer Noctrix HealthClinical Research EngineerPleasanton, CaliforniaBachelor’s degree in Engineering, Biomedical Engineering, Electrical Engineering, Computer Science, or a related technical discipline with 5+ years of relevant industry experience, or a Master’s degree with 3+ years of relevant experience. This role sits at the intersection of engineering and clinical science, contributing to software and firmware development, physiological signal processing, clinical data analysis, device characterization, verification and validation, and clinical research activities.
Sr. Manager, Clinical Data Management (Lead) Denali Therapeutics IncSr. Manager, Clinical Data Management (Lead)South San Francisco, CA$155,000–$202,000 / yearReviews and approves key clinical data management deliverables (CRF design/completion guidelines, database design specifications, data entry guidelines, data management plans, edit check specifications, SAE reconciliation plans, medical coding, data listing specifications, electronic data transfer agreements). Qualifications/Skills: Typically requires a Bachelor's degree in mathematics, science, or a health-related field and a minimum of 10 years of clinical data management experience in biotech, pharmaceutical, or health-related industries, including 3+ years of coaching/oversight experience for junior Data Management Leads.
Senior Product Manager, Clinical Platform Sprinter Health IncSenior Product Manager, Clinical PlatformMenlo Park, CAOwning our extended networks platform: You will be DRI for an exciting new initiative where we are bringing external clinical partners on-platform to expand our reach from a geography and service mix perspective while ensuring the same level of impact, quality, and patient experience of our first-party offerings. You will own those primitives: the validated patient record, the service catalog and the composition grammar that defines what a service requires and how services combine, and the authoring surface that lets a range of users stand up a new care pathway without filing an engineering ticket.
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 Imaging R&D Specialist DeepSight TechnologyClinical Imaging R&D SpecialistSanta Clara, CA$140,000–$200,000 / yearFull timeA Little About Us:DeepSight Technology Inc. is an early-stage, pre-commercial medical device company with a vision for Physical AI -scaling advanced multimodal sensing technologies so clinicians can see more, sense more, and guide procedures with greater precision and confidence. We offer a collaborative, team-oriented environment along with competitive compensation and generous benefitsIf you're highly analytical, strategic, and skilled with problem-solving, we want to hear from you!
Director, Clinical Affairs (Hybrid - Sunnyvale) Ceribell, IncDirector, Clinical Affairs (Hybrid - Sunnyvale)Sunnyvale, CAThis includes planning, designing and managing the execution of clinical trials aligned with company strategy, building and fostering relationships with key opinion leaders in the field (KOLs) and managing the preparation and dissemination of evidence through conferences, publications and marketing materials. The Ceribell System is a novel, point-of-care electroencephalography (“EEG”) platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country.
Director, Clinical Affairs Hybrid - Sunnyvale Ceribell IncDirector, Clinical Affairs Hybrid - SunnyvaleSunnyvale, CA$208,000–$256,000 / yearThis includes planning, designing and managing the execution of clinical trials aligned with company strategy, building and fostering relationships with key opinion leaders in the field (KOLs) and managing the preparation and dissemination of evidence through conferences, publications and marketing materials. The Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN''s across the country.
Sr. Director, Clinical Data Management ALX Oncology Holdings IncSr. Director, Clinical Data ManagementSouth San Francisco, CA$240,000–$280,000 / yearApproximately 12+ years of progressive Clinical Data Management experience within biotechnology, pharmaceutical, or CRO environments, including Phase I-III clinical studies, with demonstrated success leading outsourced Clinical Data Management activities, partnering across functions, and delivering high-quality clinical trial data. As the senior data management leader in a lean biotechnology environment, this individual is responsible for establishing a scalable, fit-for-purpose function that delivers high-quality clinical trial data to support development milestones, regulatory submissions, and future portfolio growth.
Manager, Field Clinical Operations Element Science IncManager, Field Clinical OperationsRedwood City, CA$150,000–$168,000 / yearAs the lead trainer and owner of the Train-the-Trainer program, the Manager will develop and maintain hands-on expertise in the Jewel patient fitting process, ensuring consistent knowledge and competency across the FCR team while remaining prepared to directly support patient fittings when needed, including during coverage gaps, new market launches, or other business needs. SUMMARY OF ROLE: The Manager, Field Clinical Operations will play a critical leadership role in the launch and scaling of Element Science's commercial operations by overseeing the performance, training, and ongoing development of the Field Clinical Representative (FCR) team.
Phlebotomist / Administrative Assistant Monday - Friday One Medical of NY, PCPhlebotomist / Administrative Assistant Monday - FridaySan Jose, CA$26.25–$28.25 / hourWhat you'll likely work on: Use impeccable C-I-CARE (a framework containing the key elements of a great interaction and effective communication that we use with patients and each other) in all patient interactions, both clinical and administrative, and ensure a fluid and positive in-office experience through patient intake, same day schedule management, appropriate follow up scheduling, strong knowledge of billing and insurance, monitoring patient feedback and assisting with outreach as necessary. Continue to care for our members beyond the lab room by answering patient messages, following up on lab cases and assisting our providers and virtual medical team with clerical duties such as, but not limited to biometric screening forms, medical record and consult review, billing inquiries, and DOH reporting.
NewContract Administrator III Revolution Medicines, Inc.Contract Administrator IIIRedwood City, CA$120,000–$150,000 / yearThe role partners with Legal, Procurement, Finance, Clinical, Research, Human Resources, and other business teams to ensure requests are complete, approvals are obtained, CLM records are accurate, and stakeholders receive timely, helpful service. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.
Pediatrics CVICU Hospitalist Clinical Instructor or Clinical Assistant Professor Stanford UniversityPediatrics CVICU Hospitalist Clinical Instructor or Clinical Assistant ProfessorStanford, CA$218,000–$245,000 / yearYour teaching duties, which will comprise approximately 5 percent of your effort and may occur in conjunction with your clinical activity, will be focused in the CVICU on clinical topics in pediatrics and pediatric cardiology, with participation in teaching Pediatric Cardiology fellows, Pediatric residents, medical students, and APPs both in the clinical setting as well as in lecture format. The pay offered to the selected candidate will be determined based on factors including (but not limited to) the experience and qualifications of the selected candidate including equivalent years in rank, training, and field or discipline; internal equity; and external market pay for comparable jobs.
Senior Clinical Research Associate Protagonist Therapeutics IncSenior Clinical Research AssociateNewark, CA$135,000–$150,000 / yearSupport study vendor management by performing key activities as delegated by study CTM, including but not limited to: Participate in evaluation of new vendors (CROs, labs, central readers, EDC, etc.) by drafting and/or reviewing RFPs, analyzing responses and drafting work orders for select vendors • Manage the day to day interactions with select study vendor(s), such as a central or specialty lab including developing training materials, lab manuals and acting as first point of contact for issue and query escalation and resolution. Part of the clinical study team and takes a lead on execution by performing key activities as delegated by the Clinical Study lead, including but not limited to: Develop and/or review key study operational documents (e.g., study reference manual, laboratory and pharmacy manuals, data management plan, query generation, monitoring plan; review site audit reports) •.
Clinical Research Coordinator, HF StratAcuity Staffing Partners IncClinical Research Coordinator, HFBurlingame, CA$50–$55 / hourThey will be comfortable collaborating with research scientists, engineers, designers, product teams, legal partners, vendors, and external collaborators to ensure successful study execution and generation of high-quality data that informs both scientific research and product development. Bachelors degree or higher in Human Factors, Human-Computer Interaction (HCI), Psychology, Cognitive Science, Public Health, Biomedical Engineering, Life Sciences, Clinical Research, or a related field involving human subjects research.
Senior Manager Clinical Affairs Intuitive SurgicalSenior Manager Clinical AffairsSunnyvale, CAThis role will oversee and manages clinical protocols and other key study documents in support of regulatory submissions; manage clinical publications and evidence dissemination strategy, oversee manage communications with clinical trial sites, CROs, KOLs and medical societies; grow, develop and manage team to interface and support all clinical requirements of the company with the applicable guidelines and regulations; foresee challenges and develops critical concepts and methodologies to overcome those. As a key cross-functional constituent, this employee will work closely with functions across the organization - Regulatory Affairs, R&D, Program Management Office (PMO), Clinical Research Engineering (CRE), Clinical Research Managers, Global Access Value Economics (GAVE), Global Public Affairs (GPA), Regulatory Compliance, Training, Legal, and commercial functions to optimize clinical study strategies to meet business objectives.
Staff Clinical Development Engineer - Incubator Intuitive Surgical IncStaff Clinical Development Engineer - IncubatorSunnyvale, CAWorking closely with physicians and cross-functional partners, you will translate clinical and technical insights into structured development plans, drive execution of clinical and preclinical evaluations, and ensure that key risks are identified and resolved. 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).
NewVeeva Vault Clinical DR Validation Support Project Manager Falcon Smart ITVeeva Vault Clinical DR Validation Support Project ManagerFoster City, CA$140,000 / yearFull timeRole Summary: We are seeking an experienced Project Manager - Responsible for planning, coordinating, tracking, and providing end-to-end project management support for the Vault Clinical Disaster Recovery (DR) Validation project, ensuring DR testing activities are completed according to the agreed scope, timeline, dependencies, and milestones. To be part of one of the most important engagements for our customer, supporting Business Process Owners and Project Managers to define, document, and deliver complex business and system requirements for the Data Strategy projects, Leads requirements refinement, including current/future state analysis, requirements documentation, prioritization, and stakeholder alignment.