NewClinical Research Coordinator Avispa TechnologyClinical Research CoordinatorStanford, CA$40–$50 / hourCoordinate oncology clinical studies from study start-up through closeout by serving as the primary contact for research participants, sponsors, and regulatory agencies, screening and consenting participants, supporting recruitment efforts, coordinating study visits, specimen collection, treatment trial activities, and monitoring study progress. Partner closely with principal investigators, clinical staff, finance teams, and sponsors to monitor study budgets, resolve billing issues, ensure patient safety, coordinate sponsor meetings, and support the successful execution of Phase I–III oncology treatment trials.
Clinical Research Coordinator Avispa Fukuoka Co LtdClinical Research CoordinatorStanford, CA$35–$40 / hourClinical Research Coordinator Responsibilities: Coordinate oncology clinical studies from study start-up through closeout by serving as the primary contact for research participants, sponsors, and regulatory agencies, screening and consenting participants, supporting recruitment efforts, coordinating study visits, specimen collection, treatment trial activities, and monitoring study progress. Partner closely with principal investigators, clinical staff, finance teams, and sponsors to monitor study budgets, resolve billing issues, ensure patient safety, coordinate sponsor meetings, and support the successful execution of Phase I-III oncology treatment trials.
Clinical Trials Research Coordinator I Artech LLCClinical Trials Research Coordinator ISan Jose, CA$30–$32 / hourAdditionally, the role involves supporting the development and implementation of routine quality control and assurance measures and providing feedback to research staff and management as instructed. Associate’s degree in Science, Public Health, Health Care Administration, or a directly related field OR a minimum of one (1) year of experience in clinical research or a directly related field.
Clinical Research Coordinator II, Clinical Trials-Santa Clara Kaiser PermanenteClinical Research Coordinator II, Clinical Trials-Santa ClaraSanta Clara, CASupports research compliance by: learning to draft and submit clinical trial applications, under guidance, in compliance and consistency with all applicable federal, state, and local regulations and KP policies and procedures; assisting with the identification of compliance and/or quality issues, escalating as necessary; implementing updates to compliance-monitoring/audit systems and documentation with guidance; learning to and performing data entry tasks with minimal supervision to assist with risk-management; implementing research protocols, procedures, and guidance to ensure confidentiality, privacy, and security of clinical research data with minimal supervision; and leveraging basic research expertise to provide guidance to investigators and other key stakeholders to ensure compliance with IRB approved protocols and local and federal guidelines. Completes work assignments by applying up-to-date knowledge in subject area to meet deadlines; follows procedures and policies, and applies data and resources to support projects or initiatives with limited guidance and/or sponsorship.
Clinical Research Engineer - Future Forward Intuitive Surgical IncClinical Research Engineer - Future ForwardSunnyvale, CACertain 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). 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. Manager Clinical Research Engineering Intuitive Surgical IncSr. Manager Clinical Research EngineeringSunnyvale, CAHire, develop and mentor CREs for the program, Presents findings to key opinion leaders, subject matter experts, physicians, and other stakeholders to identify clinical goals and translate those needs for user-centric design and development of new platforms, procedures, instruments, and accessories. Manager Clinical Research Engineering uses their in-depth clinical, scientific, and technical knowledge to lead, collaborate with engineers, physicians, user experience researchers, and other internal and external stakeholders to develop new product concepts being incubated in early exploration.
NewClinical Research Engineer Noctrix HealthClinical Research EngineerPleasanton, CA$130,000–$150,000 / yearBachelor'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.
Clinical Research Scientist LancesoftClinical Research ScientistFoster City, CA$50–$58 / hourPrimary responsibilities will include: designing, validating and performing virology, cell-based biochemical, and immunology assays;construct and propagate mutant viruses;evaluating EC50 of selected drug candidates against wt and mutant viruses;understanding MOA of lead compounds in clinical settings;interpreting results, proactively troubleshooting technical challenges and recommending potential solutions based on personal observations and/or literature searches. The ideal candidate will have hands-on experience in one or more of the following techniques: primary cell isolation and culture, ELISA, molecular biology techniques such as RNA/DNA isolation, qPCR, cloning and virus production, immune cell functional assays, and multi-color FACS.
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.
Patient Care Manager (RN), Cancer Clinical Research Stanford Health CarePatient Care Manager (RN), Cancer Clinical ResearchPalo Alto, CaliforniaClinical Practice: Ensures the effective delivery of competent, compassionate, and efficient patient care by planning, organizing, and directing the nursing services of unit(s), including the assessment of patients, implementation of physicians' orders, treatment plans and medical procedures, administration of medication and record keeping of same as well as by monitoring and evaluating patient care processes and outcomes for the patient care unit(s); coordinates nursing activities with those of other services or disciplines. The Patient Care Manager is a Registered Nurse who provides unit leadership and works in partnership with nursing, the healthcare team, hospital/system leaders to develop a quality practice setting that support professional nursing and quality patient care.
Clinical Research Scientist - I Iconma LLCClinical Research Scientist - IFoster City, CAPrimary responsibilities will include: designing, validating and performing virology, cell-based biochemical, and immunology assays; construct and propagate mutant viruses; evaluating EC50 of selected drug candidates against wt and mutant viruses; understanding MOA of lead compounds in clinical settings; interpreting results, proactively troubleshooting technical challenges and recommending potential solutions based on personal observations and/or literature searches. The ideal candidate will have hands-on experience in one or more of the following techniques: primary cell isolation and culture, ELISA, molecular biology techniques such as RNA/DNA isolation, qPCR, cloning and virus production, immune cell functional assays, and multi-color FACS.
Research Nurse III, RN, Clinical Trial - Sta. Clara Kaiser PermanenteResearch Nurse III, RN, Clinical Trial - Sta. ClaraSanta Clara, CACompletes work assignments autonomously by applying up-to-date expertise in subject area to generate creative solutions; ensures all procedures and policies are followed; leverages an understanding of data and resources to support projects or initiatives. Pursues self-development; creates plans and takes action to capitalize on strengths and develop weaknesses; influences others through technical explanations and examples.
Sr Mgr, Project Management- AI Clinical Research Kaiser PermanenteSr Mgr, Project Management- AI Clinical ResearchPleasanton, CAManages designated units or teams by translating business plans into tactical action items; oversees the completion of work assignments and identifies opportunities for improvement; ensures all policies and procedures are followed; partners with key stakeholders and business leaders to ensure products and / or services meet requirements and expectations while aligning with departmental strategies. Manages the alignment, buy-in, engagement and support of diverse project stakeholders by building and maintaining relationships as well as communicating appropriately with internal customers, third party vendors, senior and/or executive management, and business leaders; and clarifying accountability and authority across stakeholders.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorRedwood City, CA$30–$45 / hourYou will work closely with clinical staff and research teams, using technologies such as electronic medical records (EMR), electronic data capture (EDC) systems, and sleep-specific diagnostic equipment (including PSG, MWT, and actigraphy). Facilitate sleep-specific assessments such as polysomnography (PSG), Maintenance of Wakefulness Test (MWT), actigraphy, and patient-reported outcomes (PRO) or electronic clinical outcome assessments (eCOA).
Oncology Research Nursing Professional (RN), South Bay Cancer Center Stanford Health CareOncology Research Nursing Professional (RN), South Bay Cancer CenterSan Jose, CA$83.98–$111.27 / hourThe Oncology Research Nursing Professional (ORNP) -is a Registered Nurse (RN) who works collaboratively with Clinical Research Staff including, but not limited to Physicians, Clinical Research Associates (CRA), APPs, Clinical Nurses, Pharmacists, and clinic staff to coordinate care for an assigned population of patients who are enrolled into cancer center clinical research trials. The ORNP works with the PIs on the assessment, management, and coordination of research patient care across the continuum of care (outpatient, inpatient and home) including triage of phone calls and proactive patient communication.
Oncology Research Nursing Professional (Rn), South Bay Cancer Center Stanford Health CareOncology Research Nursing Professional (Rn), South Bay Cancer CenterSan Jose, CA$83.98–$111.27 / hourThe Oncology Research Nursing Professional (ORNP) -is a Registered Nurse (RN) who works collaboratively with Clinical Research Staff including, but not limited to Physicians, Clinical Research Associates (CRA), APPs, Clinical Nurses, Pharmacists, and clinic staff to coordinate care for an assigned population of patients who are enrolled into cancer center clinical research trials. The ORNP works with the PIs on the assessment, management, and coordination of research patient care across the continuum of care (outpatient, inpatient and home) including triage of phone calls and proactive patient communication.
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.
NewSr. Manager, Clinical Operations 10X Genomics IncSr. Manager, Clinical OperationsPleasanton, CA$173,100–$234,100 / yearKey responsibilities for this role include: managing a portfolio of academic collaborations and strategic partnerships according to established milestones and outcomes, leading the operational execution for large-scale, multi-year collaborations with premier academic institutions to generate evidence for future clinical applications of single-cell and spatial technologies, and driving collaboration between internal cross-functional teams and external partners to achieve desired results. Manager, Clinical Operations reporting to the Director, Business Development and Strategic Partnerships will drive the operational execution and strategic management of high-impact alliances central to 10x Genomics' effort to advance future diagnostic applications for single cell and spatial technologies.
Subject Mater Expert, Clinical Trials HCTHealthcareSubject Mater Expert, Clinical TrialsSan Jose, CAKeywords: Subject Matter Expert (SME), Clinical Trial Subject Matter Expert, Clinical Research Consultant, Clinical Research Manager, Clinical Trial Manager (CTM), Senior Clinical Trial Manager, Clinical Operations Manager, Director of Clinical Operations, Associate Director of Clinical Operations, Clinical Program Manager, Clinical Project Manager, Clinical Development Manager, Clinical Research Scientist, Clinical Scientist, Medical Affairs Manager, Research Nurse, Clinical Research Coordinator (CRC), Clinical Research Associate (CRA), Principal CRA, Clinical Trial Lead, Clinical Trials, Clinical Research, Clinical Operations, Phase I, Phase II, Phase III, Phase IV, Investigator-Initiated Trials (IIT), Multicenter Studies, Global Clinical Trials, Site Management, Trial Startup, Study Start-Up, Patient Recruitment, Site Activation, Clinical Monitoring. Experience: Minimum two (2) years of clinical nursing experience in a hospital, clinic or similar health care setting within the last three (3) years required (Bachelor’s degree may be substituted for one (1) year work experience).
Associate Scientist II (Contract), Research VaxcyteAssociate Scientist II (Contract), ResearchSan Carlos, CA$51–$56 / hourExperience with diverse protein targets, bacterial and eukaryotic recombinant proteins, small/large subunit vaccine antigens, fusion proteins, multimeric complexes, glycoproteins, and VLPs. Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked.