NewResearch And Clinical Services Specialist I Stanford Health CareResearch And Clinical Services Specialist IPalo Alto, CA$33.14–$42.25 / hourKey responsibilities include Articulates specialized information regarding services and products, provides accurate answers to inquiries, suggests alternative or supplementary product samples, and disseminates lab test results to physicians and researchers. Places orders for transfusable and non-transfusable blood products requested by the patient's physician within SHC, partner hospitals and occasionally as part of the national blood sharing group NBE.
NewResearch and Clinical Services Specialist I Stanford Health CareResearch and Clinical Services Specialist IPALO ALTO, CA$33.14–$42.25 / hourKey responsibilities include Articulates specialized information regarding services and products, provides accurate answers to inquiries, suggests alternative or supplementary product samples, and disseminates lab test results to physicians and researchers. Places orders for transfusable and non-transfusable blood products requested by the patient's physician within SHC, partner hospitals and occasionally as part of the national blood sharing group NBE.
NewClinical Nurse Manager - RN Salgado LLCClinical Nurse Manager - RNSan Jose, CA$157,000–$207,000Leadership Experience: Minimum of 2 years of experience successfully overseeing an ambulatory clinic operation (including RN, LVN, and MA staff) OR equivalent nursing leadership experience within a high-volume, outpatient setting. Team Supervision: Hire, retain, coach, develop, and supervise RN Case Managers, Clinic RNs, Medical Assistants (MAs), and other clinic team members, actively fostering an engaged and healthy workforce.
Senior Project Manager, Clinical Operations Maze Therapeutics IncSenior Project Manager, Clinical OperationsSouth San Francisco, CA$181,000–$221,000 / yearThis position combines portfolio-level project management with strategic operational initiatives, partnering closely with Clinical Operations Study Leads, Oversight Directors, and cross-functional teams to support the successful execution of multiple clinical pharmacology studies, early-phase studies, Phase 2 studies, and Phase 3 development programs, In this role, you will facilitate cross-functional planning and communication, coordinate complex study execution activities across the clinical portfolio, and oversee key Clinical Operations initiatives that strengthen organizational capabilities, improve processes, and drive operational excellence. Partner with Clinical Operations Study Leads and Oversight Directors to coordinate project management activities across multiple Phase 1, clinical pharmacology, Phase 2, and Phase 3 studies, ensuring alignment of timelines, milestones, dependencies, and cross-functional deliverables.
Director, Clinical Operations Iovance Biotherapeutics IncDirector, Clinical OperationsSan Carlos, CARemote$225,000–$240,000 / yearThis will generally involve close supervision of external contract organizations who will have responsibility for site interaction, site monitoring, data management, biostatistics, IRB interaction, central laboratory function, clinical research budget negotiation, medical writing, pharmacovigilance, and other critical activities. In depth knowledge of PC operating systems; Microsoft Office, including MS Word, MS Excel, MS PowerPoint, MS Project, MS Publisher, MS Outlook, and MS Windows NT, Exposure to CTM systems, EDC systems (eClinical, Medidata RAVE, InForm) and Safety/ Pharmacovigilance databases (ARGUS).
Trial Master File Sr. Manager, Clinical Operations Maze Therapeutics IncTrial Master File Sr. Manager, Clinical OperationsSouth San Francisco, CA$175,000–$215,000 / yearOur clinical pipeline is anchored by two small molecule programs: MZE829, an APOL1 inhibitor for patients with APOL1‑mediated kidney disease, and MZE782, which targets genetic drivers of disease in phenylketonuria (PKU) and chronic kidney disease. This role is ideal for an experienced TMF professional who thrives in a fast-paced biotech environment, enjoys building processes from the ground up, and is passionate about developing high-quality, inspection-ready Trial Master Files.
Clinical Trial Assistant Intuitive Surgical IncClinical Trial AssistantSunnyvale, CA$70,000–$94,800 / yearEstablish, organize and maintain electronic study files and trial master files, with CRO as applicable, 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.
Sr. Clinical Research Associate (Field) ShifamedSr. Clinical Research Associate (Field)Los Gatos, CaliforniaRemoteSupira Medical, a clinical-stage Shifamed Portfolio Company, is developing a low-profile, high continuous flow percutaneous ventricular assist device (pVAD) to provide temporary mechanical circulatory support in high risk percutaneous coronary interventional (HRPCI) procedures as well as patients suffering from cardiogenic shock. ABOUT SHIFAMED Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.
Accounting Manager, R&D (Non-Clinical) Summit TherapeuticsAccounting Manager, R&D (Non-Clinical)Palo Alto, California$140,000–$160,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. The Accounting Manager, R&D (Non-Clinical) plays a critical, hands-on role in owning and managing R&D accruals and expense accounting for non-clinical trial activities across a global footprint (U.S., Europe, China).
NewSenior Manager, Clinical Pharmacology & DMPK Summit TherapeuticsSenior Manager, Clinical Pharmacology & DMPKPalo Alto, California$148,000–$174,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
Interim Clinical Trial RN - 7/6/2026 AZAD Technology PartnersInterim Clinical Trial RN - 7/6/2026San Jose, CA$4,827–$5,430The Clinical Trials Nurse I (CTN-1) is a novice level position which, under the guidance and supervision of the Principal Investigator (PI) and clinical trials administrative management, assists in ensuring that the integrity and quality of the clinical trial (s) are maintained and conducted in accordance with federal, state and local regulations, Institutional Review Board (IRB) approvals, and the organizations policies and procedures. Clinical Research Professional Certificate within 12 months of hire from Society of Clinical Research Associates OR Clinical Research Associate Certificate within 12 months of hire from The Association of Clinical Research Professionals.
Sr. Director, Clinical Affairs Shifamed LLCSr. Director, Clinical AffairsLos Gatos, CA$200,000–$230,000 / yearSupira Medical, a clinical-stage Shifamed Portfolio Company, is developing a low-profile, high continuous flow percutaneous ventricular assist device (pVAD) to provide temporary mechanical circulatory support in high risk percutaneous coronary interventional (HRPCI) procedures as well as patients suffering from cardiogenic shock. This individual will own the operational, strategic, and cross-functional execution of the trial - from site activation through database lock - and will serve as the primary internal owner ensuring the study is executed on time, within budget, in full compliance with FDA and ISO 14155 requirements, and with the data integrity needed to support a successful PMA submission.
Clinical Laboratory Associate II (Thursday-Sunday) Guardant HealthClinical Laboratory Associate II (Thursday-Sunday)Redwood City, California$40–$55 / hourMinimum of Associate degree or equivalent required; Bachelor’s degree or equivalent in Biomedical Laboratory Science, Clinical Science or related field preferred; At least one year of Guardant Health Clinical Laboratory experience or equivalent high complexity and volume laboratory experience preferred; Strong computing skills; Proficiently executed Good documentation practices; Advanced knowledge of reagent stability and storage, quality control policies, and factors that influence test results; Demonstrates strong practical reasoning and sound judgment; Skilled in making informed and effective decisions; Exhibits exceptional attention to detail and a strong commitment to precision in all tasks; Strong communicator with ability to maintain open communication with internal employees, managers; Proficient in giving and receiving constructive feedback, fostering open communication and continuous improvement; Capable of independently executing tasks with minimal direction, while maintaining a collaborative approach that avoids complete isolation; Ability to divide workload evenly among CLAs in accordance with operational needs; Ability to prioritize tasks with a high emphasis on quality and time; Proactively initiate and drive projects, consistently contributing innovative solutions and seizing opportunities for process improvement; and. Work Environment: · 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; · Repetitive manual pipetting may be necessary; and.
NewContract Senior Manager, Clinical Site Budgets and Outsourcing IconmaContract Senior Manager, Clinical Site Budgets and OutsourcingSouth San Francisco, CA$91–$96 / hourAssist Clinical Development teams in defining, reviewing, validating, and negotiating vendor change orders and amendments for acceptance and execution; collaborate with Finance and Legal to provide line of sight to incremental costs for corporate planning or highlight any contractual issues. This role owns the outsourcing lifecycle for assigned US and ex-US clinical programs under client’s Clinical Development portfolio – vendor selection, financial due diligence, contract and change order negotiations, ongoing vendor performance, and spend management – in support of Clinical Development, Drug Safety, and Regulatory.
Category Manager - Clinical, Laboratory & Med/Surg Stanford Health CareCategory Manager - Clinical, Laboratory & Med/SurgPalo Alto, California$64.63–$85.65 / hourDivides category into strategic market segments and through a comprehensive market analysis (to include review of corporate financial reports, analyst calls and bleeding edge technology and product changes) develops near, mid and long range strategies for each market segment within a category of spend.b. The Category Manager, Clinical, Laboratory & Med/Surg Category Management is responsible for developing and executing sourcing and category strategies across a portfolio of medical, surgical, procedural, research, physician preference item (PPI), and clinical supply categories for Stanford Health Care and affiliated entities.
Clinical Trial Planning & Data Support LancesoftClinical Trial Planning & Data SupportFoster City, CAThe Contractor, Clinical Trial Planning & Data Support (Level C3) supports development programs by maintaining portfolio planning systems, ensuring data quality, and enabling consistent reporting across the organization. This role is aligned to Level C3 (Mid-Level Contractor / Specialist) and is expected to: Work independently within defined processes to manage planning data and system updates.
Clinical Services Manager I - Nursing for Perioperative Services (Open and Promotional) County of San MateoClinical Services Manager I - Nursing for Perioperative Services (Open and Promotional)San Mateo, CA$178,776–$223,496 / yearCurrent County of San Mateo and County of San Mateo Superior Court of California employees with at least six months (1040 hours) of continuous service in a classified regular, probationary, extra-help/limited term positions prior to the final filing date will receive five points added to their final passing score on this examination. San Mateo Medical Center is seeking a professional, goal-oriented Clinical Services Manager I to lead and oversee Perioperative Services, including the Operating Room (OR), Pre/Post-Anesthesia Care Units, Endoscopy, Sterile Processing Department (SPD), and Perioperative Scheduling.
NewClinical Nurse Manager Macpower Digital Assets Edge Private LimitedClinical Nurse ManagerSan Jose, CA$132,181–$158,617.50 / yearUnder the direction of the Clinical Services Director (CSD), the Clinical Nurse Manager organizes and directs the day-to-day operations within the clinic, oversees the clinic staff, and carefully coordinates clinic workflows to ensure effective clinical services are provided. Ensure nursing and clinic staff deliver and correctly document interventions as agreed upon in participants' care plans, including but not limited to promptly and accurately responding to physician orders, completing assessments,, and actively participating in care planning for all assigned participants.
NewRN Clinical Manager Salgado LLCRN Clinical ManagerSan Jose, CA$157,000Leadership Experience: Minimum of 2 years of experience successfully overseeing an ambulatory clinic operation (including RN, LVN, and MA staff) OR equivalent nursing leadership experience within a high-volume, outpatient setting. Team Supervision: Hire, retain, coach, develop, and supervise RN Case Managers, Clinic RNs, Medical Assistants (MAs), and other clinic team members, actively fostering an engaged and healthy workforce.
Accounting Manager, R&D (Non-Clinical) Summit Therapeutics plcAccounting Manager, R&D (Non-Clinical)Palo Alto, CAOverview of Role: The Accounting Manager, R&D (Non-Clinical) plays a critical, hands-on role in owning and managing R&D accruals and expense accounting for non-clinical trial activities across a global footprint (U.S., Europe, China). Working cross functionally with R&D, vendors, and project stakeholders across the U.S., Europe, and China, this role plays a key part in supporting global audits and statutory financial reporting in a dynamic, high growth environment.