Clinical Research Associate Integrated Resources, IncClinical Research AssociateSan Jose, CaliforniaContractorCandidate with Academic CRO experience would also be fine, leading the study(3-4 studies) Understands data management and documentation process Candidate who has worked on clinical trials as clinical data manager, CRF design and clinical data management plan, study maintenance Works with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting. Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery.
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).
Clinical Data Associate - II Integrated Resources, IncClinical Data Associate - IIFoster City, CaliforniaContractorWorks collaboratively with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting. Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery.
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.
Study Coordinator-Clinical Trials 26-00189 Alura Workforce SolutionsStudy Coordinator-Clinical Trials 26-00189San Francisco, CA$35–$40 / hourWorking closely with research teams, site staff, and study participants, this role is central to ensuring smooth study execution, accurate documentation, and sustained participant engagement throughout the trial lifecycle. The study coordinator supports the day-to-day coordination, which includes direct patient interaction and patient recruitment-related activities across decentralized and hybrid study sites.
Medical Science Liaison - Medical Devices LancesoftMedical Science Liaison - Medical DevicesSanta Clara, CA$52MSLs engage in scientific discussions, attend medical conferences, and deliver presentations to ensure that stakeholders are well-informed about the latest research and product developments. Their primary role is to disseminate scientific information, provide clinical and scientific support for products, and gather insights from the field to inform the company's strategic direction.
Scientific Manager Integrated Resources, IncScientific ManagerFoster City, CaliforniaFull timeResearch activities can include cost-of-illness evaluations, economic evaluations in clinical trials, cost-effectiveness studies, naturalistic prospective evaluations, retrospective database analyses, patient-reported outcomes research, and decision-analytic modeling. Provide high quality HEOR technical and methodological support to cross-functional teams to effectively use clinical, economic, and humanistic data to enhance value propositions, product reimbursement, and formulary access.
Program Manager III INSPYR SolutionsProgram Manager IIIMenlo Park, CA$61–$81 / hourThe Program Manager will create the program structure, oversee the complete fellow experience, strengthen the program’s reputation across targeted industries, and help drive the adoption of AI solutions within specialized domains. Information collected and processed through your application with INSPYR Solutions (including any job applications you choose to submit) is subject to INSPYR Solutions’ Privacy Policy and INSPYR Solutions’ AI and Automated Employment Decision Tool Policy: https://www.inspyrsolutions.com/policies/ .
Drug Safety Public Health Coordinator I Integrated Resources, IncDrug Safety Public Health Coordinator IFoster City, CaliforniaContractorGeneral education (high school or college) with associated and related work experience or an individual with a medico-scientific university degree. Essential Duties and Job Functions: Under the direction of immediate manager, provides troubleshooting and application support for specific applications and solutions.
Entry level Drug safety Integrated Resources, IncEntry level Drug safetyFoster City, CaliforniaContractorGeneral education (high school or college) with associated and related work experience or an individual with a medico-scientific university degree. During system implementation and change management, may support, test, and refine application configurations to align with business process needs.
Cell and Gene Therapy Technician Integrated Resources, IncCell and Gene Therapy TechnicianSan Francisco, CaliforniaContractorContribute to relevant and impactful innovation programs to enhance CART manufacturing technologies/ capabilities and work-processes (such as alternate transfection/ cell engineering strategies, media development, disposable/ closed production systems and automation) as needed/ appropriate. • Engineering degree (with appropriate Cell and Gene Therapy focus) with 4+ years of postgraduate experience (or MSc with 7+ years) in biotech/ biopharma industry (preferably in the development and characterization of manufacturing processes for cell- or gene-based therapies).
Cell & Gene Therapy Technician Integrated Resources, IncCell & Gene Therapy TechnicianSan Francisco, CaliforniaContractorEngineering degree (with appropriate bioprocessing, cell and gene therapy focus) with 4+ years of postgraduate experience (or MSc with 7+ years) in biotech/ bio-pharma industry (preferably in the development and characterization of manufacturing processes for cell- or gene-based therapies). • Contribute to relevant and impactful innovation programs to enhance CART manufacturing technologies/ capabilities and work-processes (such as alternate transfection/ cell engineering strategies, media development, disposable/ closed production systems and automation) as needed/ appropriate.
Project Manager Integrated Resources, IncProject ManagerSan Ramon, CaliforniaContractorAs and when the projects move from one developmental phase to another, the business project manager determines the target markers and eventually, designs and elaborated plan for the project. Job responsibilities: Guide the governance body, administrative board, and project unit so as to facilitate proper functioning of the project, especially at the time of initiation of the project.
Documentation Systems Manager Integrated Resources, IncDocumentation Systems ManagerFoster City, CaliforniaFull timeTitle: Documentation Systems Manager Duration: 6 Months Location: Foster City, CA The Documentation Systems Manager, Corporate Engineering provides technical leadership and accountability for all documentation systems maintenance for the engineering and research and development (R&D) laboratories, clinical manufacturing related facilities, warehouses, and office buildings at Client's Corporate Headquarters in Foster City, CA. Develops, implements, and maintains documentation programs and processes to ensure high quality of operations, and compliance with UBC, UFC, NEC codes, current Good Manufacturing Practices (GMPs), Good Engineering Practices (GEPs) and Good Laboratory Practices (GLPs).
Senior Product Manager Faro Health Inc.Senior Product ManagerSan Jose, CARemote$152,000–$179,000Design intelligent product experiences that use structured data, large language models, retrieval systems, and automation to improve customer workflows. Matter Experts, and customers to build products that solve meaningful problems across the clinical development lifecycle.
FSP Sr. CRA - Oncology Experience - US West Thermo Fisher ScientificFSP Sr. CRA - Oncology Experience - US WestFremont, CaliforniaWhat You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Contract Manager - Biotech Integrated Resources, IncContract Manager - BiotechFoster City, CaliforniaContractorKey Financial Management Activities: Key Contact for Financial Planning & Analysis Group (FP&A) Seek Monthly Confirmations from key Vendors, providing review and analysis as needed Conduct Quarterly Vendor Reviews and Business Reviews to include review of budget spent to date, discuss any pending change orders and any billing issues. Manages vendor relationships in conjunction with the other CCF functions, Clinical Operations, Bioanalytical Chemistry or Biometrics groups Works with internal customers in vendor bidding and proposal development (RFP creation and analysis) and contract management.
Clinical Project Associate II Integrated Resources, IncClinical Project Associate IIFoster City, CaliforniaContractorAssist in the maintaining clinical information and training of Clinical Operations personnel in the clinical trials database (GILDA). Assist with the planning and facilitation of investigator meeting and, when applicable, provide on location support during the meetings.
Clinical Data Associate III Integrated Resources, IncClinical Data Associate IIIFoster City, CaliforniaFull timeEssential Duties and Job Functions: Works collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists, Biomarker Statistical Programming group, Biomarker Biostatistics group, Biomarker Clinical Programming group, Biobanking and Sample Management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting. The ideal candidate should possess a BS degree or higher in a Biomedical Science or equivalent and minimum 3 years of relevant clinical data management experience and preferably along with biomarker or laboratory background and experience in a CRO or bio/pharmaceutical setting.