NewClinical Laboratory Manager - Invitae LabCorpClinical Laboratory Manager - InvitaeSan Francisco, CA$140,000–$180,000 / yearAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Clinical Research Coordinator - Division of HIV UCSF Medical CenterClinical Research Coordinator - Division of HIVSan Francisco, CAIncumbent's duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investigator's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned. The CRC will conduct screening and enrolling study participants, scheduling study visits, and will conduct all participant facing procedures including gaining informed consent, training and supporting participants on the use of the technology associated with the study, conducting study surveys, performing finger-pricks for blood spot collection, and conducting non-invasive measurements of body composition such as height, weight, waist and hip measurements.
Senior Contract Manager, Clinical Site Budgets and Outsourcing Pride GlobalSenior Contract Manager, Clinical Site Budgets and OutsourcingSouth San Francisco, CA$85–$96 / hourThis applies to direct care staff (Examples: RN, LPN, Nurse Aides, Therapists) referred to Kentucky nursing facilities, assisted living communities, or long-term care facilities, in accordance with KRS 216.793. Working knowledge of Medicare Coverage Analyses, CMS National Coverage Determinations, National Comprehensive Cancer Network (NCCN) Guidelines, and application to support and influence budget negotiations.
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 Trial Manager Contract 4D Molecular Therapeutics IncClinical Trial Manager ContractEmeryville, CA$72–$82 / hourAssist in preparation and review of clinical trial documentation such as; protocol, informed consent, Investigator Brochure, Clinical Monitoring Plan, Project Plan, Case Report Forms, Statistical Analysis Plan, Clinical Study Reports, and other study level documents. MAJOR DUTIES & RESPONSIBILITIES: Trial Management: Serve as the primary contact for managing protocol execution, including oversight of the CRO, other study service providers, and consultants that are involved in a clinical trial.
Senior Clinical Trial Manager - Job ID: 2020 Ascendis PharmaSenior Clinical Trial Manager - Job ID: 2020Palo Alto, CARemote$160,000–$170,000 / yearManages and/or supports vendor management for central laboratory, central IRB, central imaging, patient concierge services, and site payment systems including but not limited to: portal access management for sites and internal teams, report review, sample tracking, metrics review, document reviews and meeting participation. Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
NewSenior Manager / Associate Director, Clinical Operations Alto NeuroscienceSenior Manager / Associate Director, Clinical OperationsMountain View, CA$170,000–$185,000 / yearThe Senior Manager/Associate Director, Clinical Operations provides line management and functional oversight for a team of clinical trial staff spanning Clinical Trial Associate (CTA), Clinical Research Associate (CRA), Clinical Trial Manager (CTM), and Clinical Project Manager (CPM) levels. This role is responsible for staff development, workload/resource allocation across assigned studies or programs, and ensuring consistent quality and process adherence across the team, while individual contributors retain day-to-day accountability for their assigned trials.
Clinical Research Coordinator I - National Center for PTSD Palo Alto Veterans Institute for ResearchClinical Research Coordinator I - National Center for PTSDMenlo Park, CAKnowledge of VA and its health care system regarding clinical research trials and understanding of VA procedures and safety regulations; Experience with mobile and/or web analytics, dashboards, and/or processing of JSON data streams; Experience working with behavioral, mental health, and/or electronic health record data, especially using VA systems; Experience with additional data processing technologies including Python, SQL, Visual Studio, Azure, and/or AWS; Experience with AI and machine learning, particularly for behavioral data analysis; Data visualization skills. Knowledge and experience with web-based project management programs; Good interpersonal skills and strong collaborative attitude and capacity to interact with people; Strong organizational skills; Ability to work well both independently and in a collaborative team; Good writing skills and ability to develop periodic reports on program activities; Knowledge of research study protocols and IRB procedures; Knowledge and experience with manuscript development and literature review.
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.
Clinical Research Coordinator I - The Nallamshetty Lab Palo Alto Veterans Institute for ResearchClinical Research Coordinator I - The Nallamshetty LabPalo Alto, CADegree in related field; Experience with grants and contracts function, clinical trial and research data management; Experience coordinating clinical research studies, recruiting research participants, collecting research data, and working with regulatory requirements; Knowledge of clinical research principles, Good Clinical Practice (GCP), human subjects protections, and research ethics gained through education or experience is desired. The position works closely with the Principal Investigator, study team, sponsors, regulatory bodies, and research participants to ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), institutional policies, and federal regulations.
Finance Analyst (Clinical and Research) UCSF Medical CenterFinance Analyst (Clinical and Research)San Francisco, CAThe Clinical and Research Financial Analyst uses skills as a seasoned, experienced research administrator to independently develop and / or oversee research proposals, awards, and / or transactions related to contract and grant management and maintains contract and grant records in compliance with institutional research sponsor policies. The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.
Senior Director, Clinical Operations Compliance Management (GCP/Biotechnology/Oncology) Exelixis IncSenior Director, Clinical Operations Compliance Management (GCP/Biotechnology/Oncology)Alameda, CA$246,000–$349,500 / yearThe Senior Director of COCM is a key partner with our Quality Assurance team and other functional groups (including Clinical Development, Data Management, etc.) and is responsible for supporting inspection readiness activities, driving cross-study consistency in study execution and compliance with governing functional procedures and processes, and escalation of identified operational issues within development and of identified quality issues to QA. EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS: Education: Bachelor's degree in related discipline and a minimum of 15 years of related experience; or, Master's degree in related discipline and a minimum of 13 years of related experience; or, Doctoral degree in related discipline and a minimum of 12 years of related experience; or, Equivalent combination of education and experience.
Assistant Clinical Research Coordinator - Memory and Aging UCSF Medical CenterAssistant Clinical Research Coordinator - Memory and AgingSan Francisco, CAThe Assistant Clinical Research Coordinator may be responsible for the coordination of one or more single or multi-site, active or follow-up clinical studies and may help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding clinical subjects; may apply understanding of inclusion/exclusion eligibility criteria for protocols; help recruit, enroll, register, schedule and retain study subjects; record protocol specific treatments and assure collection and shipment of samples; assist research personnel to keep patients on study schedules; complete study forms to submit to sponsors and/or appropriate agencies; collect, enter and clean data into study databases, maintaining data quality; assist with data analysis; assist with preparation of reports and tables; attend team meetings; and perform other duties as assigned. Abstracts clinical data from medical records; enters data onto case report forms, study flow sheets, and other forms; submits required data and data forms in accordance with accuracy and timeliness requirements of the protocols; addresses and resolves data queries; identifies, investigates and resolves data quality issues.
Research Nurse III, RN, Clinical Trials Vallejo Kaiser PermanenteResearch Nurse III, RN, Clinical Trials VallejoVallejo, 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.
Research Nurse III, Clinical Trials - San Francisco Kaiser PermanenteResearch Nurse III, Clinical Trials - San FranciscoSan Francisco, 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.
Clinical Applications Platform Expert, Cancer Stanford Health CareClinical Applications Platform Expert, CancerPALO ALTO, CA$74.73–$99.04 / hourOn smaller efforts without a dedicated project manager assigned, may explicitly hold project-coordination responsibilities (sequencing tasks, tracking timeline, assigning work items, completing status reports) as a distinct, named responsibility layered on top of the technical platform expert role. This role exists to ensure that the organization's most complex technical, architectural, and solutioning challenges are met with consistent, well-defined expertise that can work across IT functions to examine all available tools and solutions and to bring the right combination to the design.
MGR-IT Clinical Applications Stanford Health CareMGR-IT Clinical ApplicationsPalo Alto, California$79.21–$104.97 / hourThis vibrant and innovative team delivers critical research technology solutions and services across all of Stanford Medicine (Stanford School of Medicine, Stanford Health Care, and Stanford Children’s Health).Reporting to the Director of Research Technology, this role leads a high-performing team of clinical application analysts and technical specialists responsible for the implementation, support, and continuous enhancement of our clinical research application suite—with a primary focus on Epic Research and our Clinical Trial Management System (CTMS). This role is strongly oriented towards people leadership paired with technical and business acumen to translate high-level business and clinical requirements into workflow and system solutions while managing day-to-day service delivery, SLAs, and most importantly, team performance and development.
Mgr-It Clinical Applications Stanford Health CareMgr-It Clinical ApplicationsPalo Alto, CA$79.21–$104.97 / hourReporting to the Director of Research Technology, this role leads a high-performing team of clinical application analysts and technical specialists responsible for the implementation, support, and continuous enhancement of our clinical research application suite-with a primary focus on Epic Research and our Clinical Trial Management System (CTMS). This role is strongly oriented towards people leadership paired with technical and business acumen to translate high-level business and clinical requirements into workflow and system solutions while managing day-to-day service delivery, SLAs, and most importantly, team performance and development.
Scientist (Clinical NGS) Takara Bio USA IncScientist (Clinical NGS)San Jose, CA$150,000–$165,000 / yearHow this role drives the company forward: The Scientist works primarily hands-on in the lab conducting experiments to move projects through all stages of product development; from initial Proof of Concept, through Research and Development, to Product Launch. Understands project goals, meets project specifications, and commits to deliver projects within set deadlines under guidance from Senior Scientists and colleagues in Marketing (Product Managers and/or Market Strategy Managers).
Sr. Clinical Trial Associate ALX Oncology Holdings IncSr. Clinical Trial AssociateSouth San Francisco, CA$115,000–$125,000 / yearCTA) supports clinical trial execution from study start-up through close-out, with increasing ownership of activities including Trial Master File (TMF) management, site activation, study tracking, vendor coordination, and study documentation. Support oversight of CROs and other study vendors, including tracking deliverables, timelines, documentation, system access and assisting with review of vendor and study plans; proactively identify and address routine issues and escalate risks as appropriate.