Clinical Laboratory Associate II (Thursday-Sunday) Guardant Health IncClinical Laboratory Associate II (Thursday-Sunday)Redwood City, CA$40–$55 / hourEssential Qualifications: Minimum 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.
Clinical Project Assistant Thorough GroupClinical Project AssistantSan Francisco, CaliforniaThe Clinical Project Assistant will play an important role in keeping study activities organized and on track, maintaining high-quality clinical documentation, supporting the Trial Master File, coordinating study meetings and communications, and assisting with the day-to-day operational needs of the clinical program. As the organization continues to advance its clinical development activities, they are seeking an experienced and highly organized Clinical Project Assistant (CPA) to provide operational and administrative support to Clinical Operations and the broader clinical study team.
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.
Director, Clinical Biomarkers & Translational Medicine - Oncology (Solid Tumor Portfolio) BeOne Medicines AGDirector, Clinical Biomarkers & Translational Medicine - Oncology (Solid Tumor Portfolio)San Carlos, CA$176,600–$236,600 / yearThe successful candidate will serve as the translational and biomarker lead for assigned programs, partnering closely with Discovery Research, Clinical Development, Clinical Pharmacology, Precision Medicine, Bioinformatics, Biostatistics, Regulatory Affairs, Diagnostics, Medical Affairs, and external collaborators to accelerate biomarker-driven drug development and enable data-driven clinical decision making. Working knowledge of modern translational technologies, including: next-generation sequencing (NGS), RNA sequencing, ctDNA, multiplex immunohistochemistry, digital pathology, proteomics, flow cytometry, single-cell technologies, emerging multi-omics approaches/data integration and computational biology.
Principal Scientist, Translational Clinical Biomarkers - Hematology/Oncology Merck & Co IncPrincipal Scientist, Translational Clinical Biomarkers - Hematology/OncologySouth San Francisco, CA$190,800–$300,300 / yearRequired Skills: Biomarkers, Clinical Development, Clinical Research, Ethical Compliance, Immuno-Oncology, Mechanism of Action, Oncology, Patient Care, Pharmacodynamics, Protocol Development, Research Designs, Scientific Presentations, Scientific Writing, Strategic Thinking, Translational Medicine. For solid tumors, develop strategies addressing target expression, tumor biology, molecular subtype, immune contexture, circulating biomarkers, mechanisms of response and resistance, and potential predictive biomarkers.
Director, Clinical Affairs (Hybrid - Sunnyvale) CeribellDirector, Clinical Affairs (Hybrid - Sunnyvale)Sunnyvale, CA$208,000–$256,000 / yearThis includes planning, designing and managing the execution of clinical trials aligned with company strategy, building and fostering relationships with key opinion leaders in the field (KOLs) and managing the preparation and dissemination of evidence through conferences, publications and marketing materials. The 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.
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.
Executive Director, Translational Science & Clinical Biomarkers Adicet BioExecutive Director, Translational Science & Clinical BiomarkersRedwood City, California$260,000–$359,000 / yearAdicet is located in a state-of-the-art facility and works to create an incredible office experience with an onsite gym and various other fitness options, onsite parking with electric vehicle charging stations and free shuttle (Caltrain), company-subsidized lunches (delivered onsite daily) and fully stocked breakrooms. The Executive Director will guide the design and implementation of clinical biomarker approaches to inform mechanism of action, pharmacokinetics, pharmacodynamics, patient selection, and clinical decision-making, supporting product candidates through first-in-human and subsequent clinical trials in close collaboration with cross-functional teams.
NewPrincipal Clinical Medical Writer BioMarin Pharmaceutical IncPrincipal Clinical Medical WriterCA$171,720–$236,115 / yearFilling this need with a regular full-time employee will enable BioMarin to reduce writing-related CRO and contractor costs, increase Clinical Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications. Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets.
Clinical Nursing Director - Perioperative Services Macpower Digital Assets Edge Private LimitedClinical Nursing Director - Perioperative ServicesSan Francisco, CA$199,600–$258,280 / yearEssential Responsibilities: Collaborates with CNO and other medical center management in identifying and implementing innovative models and best practices with an emphasis on quality of care, service improvements and cost reduction. Accountable for the following areas dependent upon medical center beds and services offered: Adult Services: Med Surg, Dialysis, Clinical Dietitian, Critical Care, TCU, RT, ED if applicable.
Staff II Pharmacist - Hematology/Oncology Clinical Pharmacist UCSF Medical CenterStaff II Pharmacist - Hematology/Oncology Clinical PharmacistSan Francisco, CAThese include, for example, obtaining medication histories, reviewing and assessing medication profiles, providing drug information to patients and health care providers, collaborating with clinicians on drugs of choice and therapeutic plans, ensuring access to medications, educating patients on the proper use of medications, and ensuring that patients understand cautions, adverse reactions, and interactions related to their therapy. These services include, but are not limited to: drug procurement, storage, and security; safe, accurate and timely preparation and distribution of drugs; clinical pharmacy services for patients; development of drug use policies within the Medical Center; drug information services for clinicians and patients; and participation in technology assessment and quality assurance programs.
NewSurgery Clinical Pharmacist UCSF Medical CenterSurgery Clinical PharmacistSan Francisco, CAThese include, for example, obtaining medication histories, reviewing and assessing medication profiles, providing drug information to patients and health care providers, collaborating with clinicians on drugs of choice and therapeutic plans, ensuring access to medications, educating patients on the proper use of medications, and ensuring that patients understand cautions, adverse reactions, and interactions related to their therapy. These services include, but are not limited to: drug procurement, storage, and security; safe, accurate and timely preparation and distribution of drugs; clinical pharmacy services for patients; development of drug use policies within the Medical Center; drug information services for clinicians and patients; and participation in technology assessment and quality assurance programs.
Associate Account Manager - Clinical Trial Division - West Coast, US Thermo Fisher Scientific IncAssociate Account Manager - Clinical Trial Division - West Coast, USSouth San Francisco, CA$76,700–$115,025 / yearAs one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. We equip our global teams with the tools and support they need to grow their careers while advancing science and delivering solutions to some of the world's most pressing challenges, such as protecting the environment, ensuring food safety, and helping to find cures for cancer.
Urology Clinical Nurse Manager Macpower Digital Assets Edge Private LimitedUrology Clinical Nurse ManagerSan Francisco, CA$234,000–$246,000 / yearDevelops staff in collaborative decision making and shared governance to ensure a shared voice in clinical care practice, exchange of ideas, enhanced communication, and continually improved clinical and patient care outcomes. Strong leadership, fiscal, and operations management skills, with the ability to collaborate effectively with physicians, management, and staff from all disciplines.
Mgr, Clinical Nutrition II Compass Group USA IncMgr, Clinical Nutrition IIMountain View, CAThe company has earned significant recognition, including being named one of Modern Healthcare's "Top 100 Best Places to Work in Healthcare" for five consecutive years, and appearing on Training Magazine's Top 125 Organizations list for six straight years. 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.
Senior Medical Director, Early Clinical Development BioMarin Pharmaceutical IncSenior Medical Director, Early Clinical DevelopmentCA$284,000–$390,500 / yearLeveraging deep expertise in translational clinical research and earlyâ€'phase trial design, the Senior Medical Director will lead integrated clinical development planning, design and oversee highly informative Phase 1 and Phase 2 studies, and guide key investment and governance decisions based on emerging safety, pharmacology, biomarker, and efficacy data. The role partners closely with colleagues in Early Clinical Development, Biomarkers, Clinical Pharmacology, Preclinical Safety, Clinical Safety, Regulatory, and Clinical Operations to ensure BioMarinâ€s assets are optimally positioned to generate highâ€'value insights that inform downstream development and regulatory strategy.Â.
Senior Director, Clinical Development Revolution Medicines, Inc.Senior Director, Clinical DevelopmentRedwood City, CA$244,000–$305,000 / yearHas demonstrated collaborate behaviors on enterprise-level strategic initiatives with a variety of internal and external partners and stakeholders - including clinical investigators/clinicians, scientists and key opinion leaders (KOLs), as well as internal groups, including other groups in development, research, business development, commercial, legal, etc. Represent the clinical development plan on appropriate teams, sub-teams and forums; oversee training of study site personnel, act as primary point-of-contact for questions/enquires regarding the CDP at a program level, oversee the conduct of medical/safety data reviews and study reporting.
Senior Medical Director, Early-Stage Clinical Development Revolution Medicines, Inc.Senior Medical Director, Early-Stage Clinical DevelopmentRedwood City, CA$346,000–$397,000 / yearHas demonstrated collaborative behaviors on enterprise-level strategic initiatives with a variety of internal and external partners and stakeholders - including clinical investigators/clinicians, scientists and key opinion leaders (KOLs), as well as internal groups, including other groups in development, research, business development, commercial, legal, etc. Represent the clinical development plan on appropriate teams, sub-teams and forums; oversee training of study site personnel, act as primary point-of-contact for questions/enquires regarding the CDP at a program level, oversee the conduct of medical/safety data reviews and study reporting.
Global Development Lead (Gdl), Clinical Development Revolution Medicines, Inc.Global Development Lead (Gdl), Clinical DevelopmentRedwood City, CA$369,000–$424,000 / yearPartner closely with the Project Team Leader (PTL) or Lifecycle Team Leader (LCL) to ensure that clinical development strategy, positions and decision-making are fully represented and integrated within lifecycle planning and decision-making for the molecule, with clear alignment on roles, decision rights and accountability. The GDL functions as the single point of clinical accountability for the assigned program, setting direction, driving alignment across functions, and representing the program at internal governance bodies and externally with investigators, key opinion leaders, and global health authorities.
Senior Manager, Research Informatics Revolution Medicines, Inc.Senior Manager, Research InformaticsRedwood City, CA$164,000–$205,000 / yearIn this role, you will partner closely with scientific teams, computational scientists, and technology teams to define and deliver scalable digital solutions that transform how scientific data is captured, managed, analyzed, and leveraged across the research organization. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.