NewClinical Research Coordinator ICON Strategic SolutionsClinical Research CoordinatorSanta Rosa, CACompile and maintain the clinical trial related lists and logs, including but not limited to study document version tracker, decision risk log, contact list, Q&A log, vendor list, and specific training log. The CTA supports the study team in delegated activities and provides technical, administrative and logistical support to ensure efficient execution of clinical trials in line with ICH/GCP sponsor SOP's and regulatory regulations.
Clinical Research Coordinator II, Cancer Research Sutter HealthClinical Research Coordinator II, Cancer ResearchVallejo, CA$44.34–$66.51 / hourTotal compensation considers multiple factors, including, but not limited to a candidate's experience, education, skills, licensure, certifications, departmental equity, training, and organizational needs. Possess written and verbal communications skills to communicate with fellow team members, supervisors, patients, and other hospital personnel.
Sr Research Associate 2, In Vivo for Biology Research Greenfield SourceSr Research Associate 2, In Vivo for Biology ResearchPetaluma, CaliforniaThe role includes in vivo experimentation (invention of novel models and methodology along with handling, dosing, collecting), data acquisition, data analysis and communication of experimental findings to internal teams. The ideal candidate will have a demonstrated track record on in vivo models of muscular and/or skeletal disease and will support the development and execution of in vivo PK/PD/efficacy studies from research to early development and IND submission.
Research Assistant Flourish ResearchResearch AssistantWalnut Creek, California$21–$22 / hourFlourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Support CRCs and site staff with protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.
Assistant Clinical Research Coordinator University of CaliforniaAssistant Clinical Research CoordinatorDavis, CA$32.95–$53.06 / hourMisconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. The incumbent will assist with data collection and entry, assist with participant visits, conduct recruitment activities, obtain participant medical records for abstraction, prepare study documentation, collect birth data and process and ship biological specimens, including from participant labor and delivery (cord blood and placenta).
Clinical Research Specialist Integrated Resources, IncClinical Research SpecialistSanta Rosa, CaliforniaContractorTop 3 qualifications: • Previous clinical research experience • Ability to prioritize and strong critical thinking skills • Attention to detail and strong communication skills. Qualifications: Must have ability to prioritize and critical thinking skills and previous clinical research experience.
Senior Clinical Research Scientist II Caribou Biosciences, Inc.Senior Clinical Research Scientist IIBerkeley, CA$215,000–$230,000 / yearWe believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases. Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases.
Clinical Research Coordinator II, Clinical Trials- San Rafael Kaiser PermanenteClinical Research Coordinator II, Clinical Trials- San RafaelSan Rafael, CASupports research compliance by: learning to draft and submit clinical trial applications, under guidance, in compliance and consistency with all applicable federal, state, and local regulations and KP policies and procedures; assisting with the identification of compliance and/or quality issues, escalating as necessary; implementing updates to compliance-monitoring/audit systems and documentation with guidance; learning to and performing data entry tasks with minimal supervision to assist with risk-management; implementing research protocols, procedures, and guidance to ensure confidentiality, privacy, and security of clinical research data with minimal supervision; and leveraging basic research expertise to provide guidance to investigators and other key stakeholders to ensure compliance with IRB approved protocols and local and federal guidelines. Completes work assignments by applying up-to-date knowledge in subject area to meet deadlines; follows procedures and policies, and applies data and resources to support projects or initiatives with limited guidance and/or sponsorship.
NewSenior Clinical Research Coordinator University of CaliforniaSenior Clinical Research CoordinatorDavis, CA$43.69–$70.25 / hourThe incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Team Committees (DTCs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. The UC Davis Comprehensive Cancer Center (UCDCCC) is a campus-wide multidisciplinary matrix organization whose mission is to reduce the burden of cancer among the diverse populations in our community and beyond through bidirectional engagement and transdisciplinary collaborations that enhance our understanding of cancer, inform new ways to prevent and treat cancer, and prepares a committed and inclusive workforce.
Clinical Research Coordinator Flourish ResearchClinical Research CoordinatorWalnut Creek, California$24–$33 / hourDescription Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
Medical Assistant/Research Assistant JMA Human Resources ManagementMedical Assistant/Research AssistantNovato, CAMedical Assistant/Research Assistant.
Senior Clinical Research Scientist IINewRemote Berkeley California United States Remote Caribou Biosciences IncSenior Clinical Research Scientist IINewRemote Berkeley California United States RemoteBerkeley, CARemote$215,000–$230,000 / yearWe believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases. Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases.
Senior Clinical Trials Research Coordinator University of CaliforniaSenior Clinical Trials Research CoordinatorDavis, CA$43.69–$70.25 / hourThis position works closely with principal investigators, sub-investigators, research staff, sponsors, contract research organizations (CROs), institutional review boards (IRBs), and study participants to ensure clinical trials are conducted in accordance with study protocols, Good Clinical Practice (GCP), federal and state regulations, and institutional policies. Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
Sr. Research Associate II The Steely GroupSr. Research Associate IINovato, CAThe Bioanalytical Development group seeks a highly motivated Senior Research Associate II to provide Bioanalytical and Biomarker method development in support of the Translational Research team as well as programs in non-clinical and clinical development. Our client develops, transfers and/or validate bioanalytical methods for quantifying biotherapeutic proteins, biomarkers, and anti-dug antibodies in both regulated and non-regulated environment.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedBerkeley, CA$71,900–$189,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
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.
Clinical Research Coordinator University of CaliforniaClinical Research CoordinatorDavis, CA$36.35–$58.48 / hourIn this position, the clinical research coordinator is responsible for the conduct of multiple clinical trials and research studies, including (but not limited to) recruitment, screening, enrollment (includes administering informed consent), data collection and management, study audits and monitoring visits, study closeouts, lab specimen processing, sponsor communications, and IRB and contract/budget submissions. Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
Senior Category Manager, Early Research & Development, Sourcing , San Rafael, California,Full Time (MK) Central Business SolutionsSenior Category Manager, Early Research & Development, Sourcing , San Rafael, California,Full Time (MK)San Rafael, CaliforniaThe role is primarily focused on developing and executing category strategies in the Early Research and Development area, including but not limited to the following: Preclinical Research Services Bioanalytical and Translational Sciences In-Vivo Animal Research and Toxicology Academic Research and Independently Sponsored Research The role will work with other category managers to ensure alignment on related services or overlapping suppliers supporting other categories. Stakeholder Management: align early to understand stakeholder needs, build credibility through strong relationships and solid track record of results, via a collaborative approach ability to manage senior stakeholders across various functions and foster cross-functional alignment; become the point of procurement accountability for the RED team; develop productive relationships with key suppliers.
Senior Research Associate Onyx BioSenior Research AssociateBerkeley, California$100,000–$130,000 / yearIn practice, you will work across our entire operation depending on need and priority: you’ll be supporting our sample collection kit/biobanking operations at times, and also running single-cell genomics and multiomics assays to support data generation at other times. You will work alongside two senior teammates—one leading R&D and assay development, the other leading platform/operations—providing the precise, reliable execution that turns precious patient samples into clean, reproducible multiomics data.
RESEARCH SCIENTIST State Of CaliforniaRESEARCH SCIENTISTMartinez, CA$6,942–$9,799If you are unable to submit your application electronically through your CalCareers account, please email apply@cdph.ca.gov for assistance and a CDPH Human Resources Division staff member will contact you to assist with the online application process or, a hard copy application package may be submitted through an alternative method as explained in the How to Apply section below. The role ensures that testing activities within the Technical/General Supervisor Section of the high-complexity Clinical Laboratory Improvement Amendments (CLIA) certified genetic screening laboratory are conducted in compliance with established quality assurance protocols.