Clinical Research Jobs in Stanford, CA
Itlearn360
Menlo Park, CA
Summit has begun its clinical development of ivonescimab in non-small cell lung cancer (NSCLC), with three active Phase III trials: HARMONi is a Phase III clinical trial which intends to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who have progressed after treatment with a 3rd generation EGFR TKI (e.g., osimertinib). Ivonescimab, known as SMT112, is a novel, potential first-in-class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule.
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.
Stanford Blood Center
Redwood City, CA
The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs. The Department of Orthopaedic Surgery is looking for a Clinical Research Coordinator Associate (CRCA) to participate in the coordination of multiple clinical and translational research projects involving the diagnosis of osteoarthritis as we as outcomes after total join replacement and fracture care.
Summit Therapeutics Sub, Inc.
Menlo Park, CA
This role will collaborate with functional team members, CROs, and vendors to successfully deliver clinical studies under direction from Clinical Trial Manager or Director. Directs and completes communication between the project team and site personnel to ensure that they are appropriately trained, remain current with project requirements, and have a thorough understanding of study milestones and deliverables.
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.
Avispa Technology
Palo Alto, CA
The successful candidate will primarily collect/manage patient and laboratory data for clinical research projects, manage research project databases, develop flowcharts and other study-related documents, and complete study documents and case report forms. Clinical Research Associate Responsibilities: Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
Itlearn360
Sunnyvale, CA
It would be a plus if you also possess previous experience in:Experience with in vitro diagnostic clinical trials; Knowledge of GCP, ICH guidelines, and FDA regulations; Previous hands-on experience in clinical research at either a diagnostic company, hospital or laboratory; Previous experience as a clinical trial assistant or equivalent; Experience with electronic trial master file (eTMF) tools. Collect and review in-house and on-site Trial Master File (TMF), product accountability logs, study supplies inventory, case report forms, and source documents for completeness, accuracy, consistency and compliance; identifies deficiencies and discrepancies and provides remedial training and/or corrective action as required.
Stanford University
Redwood City, CA
The Department of Orthopaedic Surgery is looking for a Clinical Research Coordinator Associate (CRCA) to participate in the coordination of multiple clinical and translational research projects involving the diagnosis of osteoarthritis as well as outcomes after total joint replacement and fracture care. The CRCA will perform duties related to the coordination of clinical studies, consent patients in person, interview patients, monitor follow-up, coordinate collection of clinical data and research samples as well as ensuring compliance and safety under the supervision of the principal investigator.
PAVIR
Palo Alto, CA
Manage study correspondence; Complete all study logs and case report forms; Communicate with Sponsor and Primary Site as needed, obtain and archive all regulatory documents required by Sponsors; Maintain IRB approval; Enroll patients, obtain informed consents, as well as all clinical data for study subjects; Coordinate patient visits; Coordinate any Sponsor visits; Administer neuropsychological tests, questionnaires, and collect medical information according to the study protocols. Maintain study binders containing clinical patient data; Enter all study data into research database; Maintain all electronic and paper files; Maintain data and coordinate data entry on Sponsor's online data entry sites; Perform other research related duties as needed.
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.
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.
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.
Stanford University
Palo Alto, CA
The Algorithm-Led Patients Activated in Cancer Care Through Teams (A-PACT) Study will evaluate whether a lay health worker-led intervention, combined with a machine learning algorithm to identify high-risk cancer patients, reduces hospitalizations, emergency department visits, and intensive end-of-life care. The EMBRACE study (Equity in Metastatic Breast Cancer through Community Engagement) is a prospective, randomized trial designed to evaluate the effectiveness of a multi-level intervention aimed at improving patient activation, shared decision-making (SDM), and clinician-patient communication among low-income and minority patients with metastatic breast cancer.
WorldLink, Inc.
Mountain View, CA
Whileperforming the duties of this job, the contract employee isoccasionally required to stand, clean, crawl, kneel, sit,sort, hold, squat, stoop, stand, twist the body, walk, usehands to finger, handle, or feel objects, tools orcontrols, reach with hands and arms, climb stairs or laddersand scaffolding, talk or hear, and lift up to 20 pounds. From customsoftware development to cloud hosting, from big datato cognitive computing, we help companies harnessand leverage today’s most cutting-edge digitaltechnologies to create value and grow.
Johnson & Johnson
Milpitas, CA
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. In 2017, J&J expanded into cataract surgery, laser refractive surgery (LASIK), and consumer eye health, serving more than 60 million patients a day across 103 countries with its eye health portfolio.
Wal-Mart
Mountain View, CA
Top 3 Skills for an ideal person:Human subject research (data collection on subjects, clinical research in universities),clinical protocols (drafting &reviewing), Data management & monitoring with experience in Sleep Research. Develops product-critical physiological data-collection protocols and executes studies according to good laboratory practice, following applicable health and safety principles and practices.
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.
The Fountain Group
Mountain View, CA
Tasks include: protocol development, clinical documentation, training sites, data collection, and clinical data manual writing. Day-to-Day ResponsibilitiesExecute end-to-end clinical studies under IRB protocol.