Medical Director, Clinical Research Cardiovascular Cytokinetics IncMedical Director, Clinical Research CardiovascularSouth San Francisco, CA$276,120–$322,140 / yearCytokinetics 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. The individual will also partner with members of the new product planning group to assist with market research, defining the target product profile, and health economics and outcomes research, as well as serving as a consultant to evaluate new projects in research and outside licensing opportunities.
Medical Director, Clinical Research Neuromuscular Cytokinetics, IncorporatedMedical Director, Clinical Research NeuromuscularSouth San Francisco, CA$276,120–$322,140 / yearMD or MD/PhD degree with internal medicine or neurology board certification by the American Board of Internal Medicine with a minimum of 2+ years of experience in clinical development, either in a biotechnology or pharmaceutical company or as a clinical investigator, including industry-sponsored multi-center trials. 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.
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.
Research Associate – Biology II Integrated Resources, IncResearch Associate – Biology IIFoster City, CaliforniaFull timeLaboratory experience in biological sample managementExperience in biological sample data curationExperience in facilitating and managing quotes and contracts from external service vendorsExperience using Excel and/or scientific/clinical databases; database validation experience a plus. Job DescriptionJob Title: Research Associate – Biology IILocation: Foster City, CA 94404Duration: 6 MonthsProvide operational support for acquisition and management of human biological samples collected for biomarker and other research purposes to help achieve the goals of the Biomarker Sciences Group.
Clinical Data Associate - II Integrated Resources, IncClinical Data Associate - IIFoster City, CaliforniaContractorClinical Data Associate - IIWorks 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.
Research Associate - Biology Integrated Resources, IncResearch Associate - BiologyFoster City, CaliforniaFull timeJob DescriptionTitle: Research Associate - Biology - IILocation: Foster City, CA, United StatesDescription:Plans and executes assigned experiments that support research activities and project goals. Research Associate - BiologyIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Senior Manager Clinical Affairs Intuitive Surgical IncSenior 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.
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.
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.
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 Trial Assistant Intuitive Surgical IncClinical Trial AssistantSunnyvale, CA$70,000–$94,800 / yearEstablish, organize and maintain trial master file and clinical trial management system 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.
Research Associate – Biology Integrated Resources, IncResearch Associate – BiologyFoster City, CaliforniaContractorPlan, schedule and perform on-site receiving, accessioning, and distribution of samples from commercial vendors and academic collaborators as well as clinical studies and Investigator Sponsored Trials (ISTs) to fulfill approved sample requestsMonitor sample delivery, sample quality, and performance of vendor according to contractMaintain information on sample vendors regarding inventory, sample costs, sample collection services and performancePerform biomarker sample aliquoting to conserve samples on request and barcode and accession child samples into inventory. Laboratory experience in biological sample managementExperience in biological sample data curationExperience in facilitating and managing quotes and contracts from external service vendorsExperience using Excel and/or scientific/clinical databases; database validation experience a plus.
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.
Senior Clinical Study Manager Intuitive Surgical IncSenior Clinical Study ManagerSunnyvale, CAAccountable for the planning and execution of the clinical studies including site selection, review of potential patient recruitment and projections, creation of study related documents (protocols, case report forms, Informed consents, Clinical trial agreements, study reports), organizing IRB/EC submissions with follow-thorough to ensure successful progress. As a member of the Clinical Affairs team, this role will be accountable for working with key stakeholders to design and develop clinical protocols and other key study documents, effectively interact with key opinion leaders (KOLs) and execute clinical studies (pre-market or post-market studies), independently and with minimal supervision.
Postdoctoral Fellow - Next-Gen Sequencing Systems, Research & Early Development F. Hoffmann-La Roche LtdPostdoctoral Fellow - Next-Gen Sequencing Systems, Research & Early DevelopmentSanta Clara, CA$100,000–$106,000 / yearJoining our Systems Technology Group, you will play a major role in the Research and Early Development of new technology, devices, and instruments associated with our next-generation DNA sequencing and molecular diagnostic platforms. You will develop and implement microfabrication processes, including photolithography, etching, drilling, bonding, and dicing-and utilize precision metrology instruments to characterize components and evaluate manufacturing methodologies.
NewLife Sciences Research Associate II - Regenerative Medicine PAVIRLife Sciences Research Associate II - Regenerative MedicinePalo Alto, CAFull timeQUALIFICATIONS Required: PhDAt least three years of prior research experience in biology, bioengineering, cell biology, molecular biology or a related discipline (can include during studies);Advanced knowledge of scientific research methodology;Ability to troubleshoot an experiment as necessary;Exquisite record keeping and experimental documentation capabilities;Excellent organizational skills;Strong scientific writing skills and demonstrated capacity to drive first author publications;Knowledge of safe handling/storage of biohazardous chemicals & bloodborne pathogens;Solid training in general lab skills such as micro-pipetting, PCR analysis, genomic and plasmid DNA preparation, protein measurements, and tissue homogenization;Solid training in biomaterials fabrication and characterizationSolid training in analytical skills, including routine calculations of dilution factors and solution concentrations as well as using Excel and other programs for data calculation and analysis;Knowledge of research procedures and protocols gained through education or experience;Experience in a variety of research techniques/methods and follow-up data collection;Knowledge of laboratory safety rules and procedures;Excellent communication skills (written and verbal), including public speaking skills;Ability to work independently and proactively;Ability to work within a team context and collaborate with other lab personnel. on the design and execution of laboratory experiments; Serve as the main contact for experiments;Develop and validate experimental protocols;Analyze data from experiments; Prepare charts for presentations and publication;Write papers on projects for publication;Perform general lab organization; Guide and train lab technicians.
NewLife Sciences Research Associate – Regenerative Medicine PAVIRLife Sciences Research Associate – Regenerative MedicinePalo Alto, CAFull timeStrong scientific writing skills and demonstrated capacity to drive first author publications;Knowledge of safe handling/storage of biohazardous chemicals & bloodborne pathogens;Solid training in general lab skills such as micro-pipetting, PCR analysis, cell culture, immunofluorescence staining, and biomaterials characterization;Solid training in analytical skills, including routine calculations of dilution factors and solution concentrations as well as using Excel and other programs for data calculation and analysis or biostatistical analysis;Knowledge of research procedures and protocols gained through education or experience;Experience in a variety of research techniques/methods and follow-up data collection;Knowledge of laboratory safety rules and procedures;Excellent communication skills (written and verbal), including public speaking skills;Ability to work independently and proactively;Ability to work within a team context and collaborate with other lab personnel. on the design and execution of laboratory experiments; Serve as the main contact for experiments;Develop and validate experimental protocols;Analyze data from experiments; Prepare charts for presentations and publication;Write papers on projects for publication;Perform general lab organization; Guide and train lab technicians or other lab members;Other research activities as assigned.
Sr. Clinical Study Manager Intuitive Surgical IncSr. Clinical Study ManagerSunnyvale, CAAccountable for the planning and execution of the clinical studies including site selection, review of potential patient recruitment and projections, creation of study related documents (protocols, case report forms, Informed consents, Clinical trial agreements, study reports), organizing IRB/EC submissions with follow-thorough to ensure successful progress. The candidate will be required to work closely with clinical research associates (CRAs), clinical trial assistants (CTAs) and data management for the conduct and execution of the study, as well as with biostatisticians to review and interpret results of clinical studies, develop clinical study reports, or help the development of clinical publications.