Clinical Data Manager AccuScan SciencesClinical Data ManagerMilpitas, CAThe CDM will play a critical role in supporting clinical data pipelines, investigating anomalies, and driving MRD-focused analyses, pipeline improvements, and research initiatives. This role ensures data integrity, identifies and resolves irregularities, and partners closely with laboratory operations and bioinformatics engineering to enable high-quality and timely data delivery.
Clinical Project Manager Alto Neuroscience IncClinical Project ManagerMountain View, CA$125,000–$170,000 / yearCoordinate and contribute to the development of clinical study documents, including protocols, Investigator's Brochures (IBs), informed consent forms (ICFs), case report forms (CRFs), study plans, status reports, and clinical study reports. Foster cross-functional collaboration by guiding, influencing, and supporting team members outside of direct reporting lines to ensure alignment, knowledge sharing, and consistent execution of clinical operations priorities.
Registered Nurse (RN) Clinical Manager - ICU/ER Macpower Digital Assets Edge Private LimitedRegistered Nurse (RN) Clinical Manager - ICU/ERManteca, CA$123,219–$165,838 / yearJOB SUMMARY: The Clinical Manager (Registered Nurse) is accountable for assisting the Director in providing leadership to the Emergency and Intensive Care Services Departments in the areas of leadership, clinical, financial, and human resources. Accountable for assisting in planning, organizing, implementing and evaluating nursing practice in accordance with the Mission of Doctors Hospital and Emergency Department and Intensive Care Unit.
Clinical Account Manager - New England (Sales) Becton Dickinson and CoClinical Account Manager - New England (Sales)Milpitas, CARemoteAs part of the Waters Biosciences Commercial team, drive sustainable territory growth by developing new business opportunities, expanding strategic clinical accounts, and advancing customer adoption of Waters solutions across clinical and diagnostic testing environments. Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance.
Clinical Flow Cytometry Account Manager - South Texas Becton Dickinson and CoClinical Flow Cytometry Account Manager - South TexasMilpitas, CARemoteAs part of the Waters Biosciences Commercial team, drive sustainable territory growth by developing new business opportunities, expanding strategic clinical accounts, and advancing customer adoption of Waters solutions across clinical and diagnostic testing environments. Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance.
Clinical Nurse Manager Healogics IncClinical Nurse ManagerAntioch, CAOrganizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licensed Practical Nurses (LPNs) or Licensed Vocational Nurses (LVNs); Certified Medical Assistants (CMAs); Hyperbaric Oxygen Technicians, etc. May be required to provide case management to a group of patients providing specific assessments according to protocols and procedures, clinical competence in procedural skills, treatments, and patient/caregiver education related to wound care management.
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.
Clinical Monitoring Oversight Manager - Contractor Arcus Biosciences, Inc.Clinical Monitoring Oversight Manager - ContractorHayward, CARemoteThe Clinical Monitoring Oversight Manager will work with Study Management Teams (SMT) to support Study Planning and Execution with drafting, implementing, and review of monitoring related study plans, identifying monitoring performance issues, managing site quality matters, assessing data quality metrics, documenting potential risks, escalating appropriate risks and issues, and communicating necessary action plans with cross functional Study Management Team. For blinded studies, the CMOM may act as the lead unblinded Clinical Operations contact, supporting unblinded study processes and associated oversight of monitoring expectations, including but not limited to the investigational product (IP) handling and accountability, management of the IXRS/IRT system, management of protocol deviations and unblinded safety reports, and documentation associated with these activities.
Clinical Monitoring Oversight Manager - Contractor Arcus Biosciences IncClinical Monitoring Oversight Manager - ContractorHayward, CARemoteThe Clinical Monitoring Oversight Manager will work with Study Management Teams (SMT) to support Study Planning and Execution with drafting, implementing, and review of monitoring related study plans, identifying monitoring performance issues, managing site quality matters, assessing data quality metrics, documenting potential risks, escalating appropriate risks and issues, and communicating necessary action plans with cross functional Study Management Team. For blinded studies, the CMOM may act as the lead unblinded Clinical Operations contact, supporting unblinded study processes and associated oversight of monitoring expectations, including but not limited to the investigational product (IP) handling and accountability, management of the IXRS/IRT system, management of protocol deviations and unblinded safety reports, and documentation associated with these activities.
Clinical Laboratory Scientist (CLS) - Travel/Contract - Up to $2,550/week! Connected Health Care, LLCClinical Laboratory Scientist (CLS) - Travel/Contract - Up to $2,550/week!San Jose, CAConnected Health Care, a premier recruitment and staffing firm, is partnering with a respected healthcare client near San Jose, California, to hire an experienced Local Travel Clinical Laboratory Scientist (CLS) for a 4-month contract assignment. Easy Access: Short drive to Monterey Bay, Santa Cruz beaches, and downtown San Jose for weekend getaways .
Associate Clinical Trials Administrator Procept Biorobotics CorpAssociate Clinical Trials AdministratorSan Jose, CA$82,110–$96,600 / yearIt continues with our one-of-a-kind management program designed to build the best managers in the industry, where our people managers across functions come together to exchange ideas and grow, as both managers and learners, in an environment that challenges, supports and broadens. It starts with our live induction program that serves as an incubator for cross-functional team building, an immersion in Procept's history, jam-packed interactive sessions with executive leadership and a crash-course in the mission and purpose of what we do.
Clinical Affairs Associate Manager Rodan & Fields, LLCClinical Affairs Associate ManagerSan Ramon, CA$84,000–$105,000 / yearThe Clinical Affairs Associate Manager will partner closely with Product Development and R&D to assist with designing and implementing comprehensive testing plans to validate new ingredients/technologies during early development all the way through final clinicals to validate product performance and safety. Manage all aspects of study execution with external research partners including but not limited to protocol development, drafting questionnaires, preparing IRB documentation, labeling and shipping samples, managing purchase orders and contracts.
Clinical Researcher Ceribell, IncClinical ResearcherSunnyvale, CA$127,000–$140,000 / yearThe 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. You will be the central point of contact for our research partnerships, ensuring the scientific integrity, smooth execution, and successful completion of critical projects that drive our product and clinical evidence development.
Clinical Researcher CeribellClinical ResearcherSunnyvale, CA$127,000–$140,000 / yearThe 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. You will be the central point of contact for our research partnerships, ensuring the scientific integrity, smooth execution, and successful completion of critical projects that drive our product and clinical evidence development.
Mgr, Clinical Nutrition I Compass Group USA IncMgr, Clinical Nutrition IHayward, CA$105,000–$120,000 / yearResponsible for managing daily clinical operations, ensuring regulatory compliance, supporting quality and patient care initiatives, mentoring dietitians, collaborating with multidisciplinary leadership, and driving operational excellence across multiple hospital locations. Compass Group employs over 3,000 RDNs across the United States, making us one of the nation's largest employers of Dietitians in a variety of settings: Hospitals and healthcare systems.
NewSenior Project Manager/Clinical Evaluation Reporting (on-site) AbbottSenior Project Manager/Clinical Evaluation Reporting (on-site)Pleasanton, South CarolinaThe primary function of a Regulatory Project Manager, Clinical Evaluations (“Clinical Evaluation Report (CER) Project Manager (PM)”) is to combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with EU MDR 2017/745, MEDDEV 2.7/1 Rev 4, MDCG Guidance documents, and predicate MDD and AIMDD directive requirements. Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D, Clinical R&D, A&P and Marketing, Library Services, Quality Engineering, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers).
NewSenior Project Manager/Clinical Evaluation Reporting (on-site) Abbott LaboratoriesSenior Project Manager/Clinical Evaluation Reporting (on-site)Pleasanton, CA$90,000–$180,000 / yearThe primary function of a Regulatory Project Manager, Clinical Evaluations ("Clinical Evaluation Report (CER) Project Manager (PM)") is to combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking of new devices and maintaining of CE Mark for existing devices in accordance with EU MDR 2017/745, MEDDEV 2.7/1 Rev 4, MDCG Guidance documents, and predicate MDD and AIMDD directive requirements. Facilitate communication and exchange of documents between stakeholders (e.g., internal personnel such as Regulatory Affairs, R&D, Clinical R&D, A&P and Marketing, Library Services, Quality Engineering, Clinical Affairs, Risk Management, Program Management, as well as external vendors such as CROs, Medical Writers and Physician Reviewers).
MGR, CLINICAL NUTRITION I Compass Group North AmericaMGR, CLINICAL NUTRITION IHayward, CA$105,000–$120,000 / yearResponsible for managing daily clinical operations, ensuring regulatory compliance, supporting quality and patient care initiatives, mentoring dietitians, collaborating with multidisciplinary leadership, and driving operational excellence across multiple hospital locations. Compass Group employs over 3,000 RDNs across the United States, making us one of the nation's largest employers of Dietitians in a variety of settings: Hospitals and healthcare systems.
DRG Clinical Validation Lead Elevance HealthDRG Clinical Validation LeadWalnut Creek, CA$89,520–$161,136 / yearPreferred Skills, Capabilities and Experiences: One or more of the following certifications are preferred: Registered Health Information Technician (RHIT), Registered Health Information Administrator (RHIA), Certified Clinical Documentation Specialist (CCDS), Certified Documentation Improvement Practitioner (CDIP), Certified Professional Coder (CPC) or Inpatient Coding Credential such as CCS or CIC. How you will make an impact: Conducts pre-certification, retrospective, out of network and appropriateness of treatment setting reviews to ensure compliance with applicable criteria, medical policy, and member eligibility, benefits, and contracts.
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!