Clinical Research Jobs in San Francisco, CA
University of California
San Francisco, CA
Your work will employ a wide range of cutting-edge techniques, including CRISPR screening, human cell culture, cloning, flow cytometry, protein assays, RNA sequencing (RNAseq), RNA interference (RNAi), single-cell analysis, and mouse models. Dr. Momen-Heravi’s research employs a multidisciplinary approach that integrates population-based studies, translational research, and computational and experimental strategies to study cancer and periodontal disease, aiming to identify biomarkers and actionable molecular targets.
Nudge Real Estate
San Francisco, CA
The Research Team at Nudge is innovating on multiple frontiers in neuroscience and neurotechnology, and is primarily focused on developing ultrasound-based neuromodulation to treat conditions like depression, chronic pain and addiction as well as enhance the wellbeing of healthy people. To realize those ambitions, we’re growing a scrappy, multidisciplinary, science and engineering team focused on making the best technology possible for interfacing with the whole brain, and a product that has the potential to improve people’s daily lives more than any other.
MedChi, The Maryland State Medical Society
Oakland, CA
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TANNER & ASSOC INC
San Francisco, CA
Develop initial clinical designs for future trials, collaborating with research, translational oncology, biostatistics, clinical operations, regulatory, and pharmacology teams, and presenting at Therapeutic Development Team meetings. Tanner and Associates is recruiting several Medical Directors of Oncology Clinical Research for major biotech companies located in San Francisco, Los Angeles, Salt Lake, and New Jersey.
Direct Staffing Inc
Emeryville, CA
Years of Experience:Typically requires 5 years of experience in clinical research, including a minimum of 2 years field monitoring experience and 3 years in lead CRA role. Excellent knowledge of medical terminology, protocol, clinical trial process, regulatory requirements, & company SOPs.
Abbott Laboratories
$79500 - $138700 undefined
Alameda, CA
Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.
TANNER & ASSOC INC
San Francisco, CA
Medical monitoring of Phase I-III trials including serving as the primary Clinical Science contact on the Protocol Execution Teams(s) and the primary liaison for clinical operations and the primary point of contact for Medical Monitor inquiries from sites, monitors and CROs. Provide initial clinical designs for future trials including partnering with research, translational oncology, biostatistics, clinical operations, regulatory and pharmacology for input/alignment and presentation at the Therapeutic Development Team meetings.
Inria
San Francisco, CA
With a presence in the fields of computational neuroscience and biology, data science and modeling, software engineering and certification, as well as collaborative robotics, the Inria Centre at Université Côte d'Azur is a major player in terms of scientific excellence through its results and collaborations at both European and international levels. For example, a simple inference delivery strategy is to provide the inference from the local AI model if this seems to be accurate enough or to forward the input to a more accurate model at a different node if the inference quality improvement compensates for the additional delay or resource consumption.
Horizon3 AI
San Francisco, CA
We're committed to helping solve our common security problems: ineffective security tools, false positives resulting in alert fatigue, blind spots, “checkbox” security culture, cybersecurity skills shortage, and the long lead time and expense of hiring outside consultants. Our flagship product, the NodeZero platform, delivers production-safe autonomous pentests and other key assessment operations that scale across the largest internal, external, cloud, and hybrid cloud environments.
Abbott Laboratories
$86700 - $173300 undefined
Alameda, CA
Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.
Abbott Laboratories
$72100 - $114700 undefined
Alameda, CA
The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155. Demonstrate excellence in teamwork, solid interpersonal and communication skills including building rapport with team members/peers, study site staff, and clinical management.
Genentech
San Francisco, CA
Alongside the Clinical Science Leader (CSL)/Global Development Leader (GDL), the Senior Clinical Scientist leads the development of the clinical science aspects of the Clinical Development Plan (CDP) strategy and supports various deliverables for effective and efficient CDP execution for the molecule/indication. You have 6+ years academic and/or industry experience, with a primary focus in late stage clinical development; you have the ability to independently carry out the majority of their study conduct responsibilities and clear evidence of independence with respect to clinical science oversight and setting out the clinical science strategy to the clinical sub team.
OpenSpecimen (Krishagni)
San Francisco, CA
The CRC’s duties may include, but will not be limited to supporting the management and coordinating the tasks of multiple clinical research studies; maintaining and updating research databases and reports; managing protocols in the Committee on Human Research online system (IRIS), including renewals and modifications of protocol applications and the implementation of new studies; assuring compliance with all relevant regulatory agencies; maintaining regulatory documents; reporting study progress to investigators; and other duties as assigned. Under the supervision of Dr. Michael Wilson and Dr. Joseph DeRisi, the CRC will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols; coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
TalentBurst, Inc.
$60 - $65 HOUR
CA, CA
The candidate will be required to work closely with clinical study managers, 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, contribute to clinical study reports, or help the development of clinical publications. Manage site start-up/activation process, including: Heavy contribution to the preparation of study-related documents (protocols, case report forms (CRFs) or eCRFs, draft informed consent forms (ICF) and complete checklists, able to help clinical trial agreements and budget negotiation, clinical monitoring plan).
Horizon3 AI, Inc.
San Francisco, CA
We’re motivated to create a safer, more secure environment, convert new ideas to exceptional solutions and great customer experiences. From intern to CEO, we celebrate diversity and bring a wide array of experience from technology startups, Fortune 500s, and the US Military.
SoftBank Investment Advisers (SBIA)
Redwood City, CA
By unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide. The company’s platform is already delivering unprecedented insights into the microbial landscape, providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood, and helping industry accelerate the development of therapeutic solutions.
UNAVAILABLE
San Francisco, CA
The California Pacific Medical Center Research Institute supports a comprehensive liver disease research program that provides patients access to many clinical trials focused on innovative therapies, devices, and antiviral agents in the areas of viral hepatitis, nonalcoholic liver disease, autoimmune liver diseases, portal hypertension, liver cancer and liver transplantation. The liver disease management and transplant team at CPMC has achieved national recognition in patient outcomes and research, including the following distinctions: • Recognized by the Scientific Registry of Transplant Recipients in 2014 as the only liver and kidney transplant program in the nation to exceed better-than-expected patient outcomes.•
Utah State Extension
San Francisco, CA
The California Pacific Medical Center Research Institute supports a comprehensive liver disease research program that provides patients access to many clinical trials focused on innovative therapies, devices, and antiviral agents in the areas of viral hepatitis, nonalcoholic liver disease, autoimmune liver diseases, portal hypertension, liver cancer and liver transplantation. Serves as one of 15 sites in the United States selected to participate in the National Institutes of Health's Hepatitis B Research Network, bringing together clinical centers with expertise in caring for patients with chronic hepatitis B virus infection.