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Reporting to the Gynecologic Oncology Clinical Research Manager, the Clinical Research Coordinator 2 will conduct industry-sponsored trials, cooperative group trials, and investigator-initiated clinical research studies, from start-up to close-out.
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Assisting with all phases of patent litigation, including discovery, depositions, hearings, and trials. Firm Type: Law Firm, Experience: 2 Years, A law firm in Palo Alto, CA, is seeking a Patent Litigation Associate Attorney with 2-5 years of experience.
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Provides subject expertise on a diverse portfolio of development programs and different therapeutic modalities including small molecules, biologics and cell gene therapy for Gilead's global clinical trials.
$355,410 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Lead the design, development, and production of new silicone/plastic injection mold tooling (including optimization trials and DOEs) to meet strict part and assembled device requirements. 5+ years experience with a wide range of molding techniques including multiple of the following: insert molding, 2 shot molding, die casting, transfer molding, liquid silicone molding, and thermoforming.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Support in all phases of patent litigation including discovery, trial, and appeal, and will include lead paralegal support at trials and hearings. Assist with preparation for depositions, witness interviews, hearings, trials, and arbitration.
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Plan and perform components of process development and technology transfer for manufacturing of clinical cell therapies, scale-up/scale-out and optimization activities in transitioning and translating pre-clinical, benchtop research into phase appropriate clinical trials.
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The Oncology Research Nursing Professional (ORNP) –is a Registered Nurse (RN) who works collaboratively with Clinical Research Staff including, but not limited to Physicians, Clinical Research Associates (CRA), APPs, Clinical Nurses, Pharmacists, and clinic staff to coordinate care for an assigned population of patients who are enrolled into cancer center clinical research trials.
$81.53 - $108.02 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Synthego's mission is to enable agile life science research and development from discovery through clinical trials by providing scientists with comprehensive CRISPR solutions for each phase coupled with full technical and regulatory support from industry-leading experts.
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Reporting to the Gynecologic Oncology Clinical Research Manager, the Clinical Research Coordinator 2- will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge.to conduct industry sponsored trials, cooperative group trials, investigator initiated clinical research studies, from start up to close out.
$92,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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This team runs clinical trials for a wide range of disease areas including: Epilepsy, Neuroimmunology/Multiple Sclerosis, Alzheimer's, Autonomic Disorders, Device Neurosurgery, Stem Cell Neurosurgery, Headache, Radiology, Parkinson's and more.
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The Advanced Analytics team within Clinical Data Sciences is seeking a Director of Data Science to act as product manager for AI-Driven clinical trials to work with clinical development and clinical operations to define, scope, and understand what key AI and analytics capabilities are needed to drive the optimization of clinical trials.
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Reporting to The Thoracic Oncology Clinical Research Manager, the Clinical Research Coordinator 2 will conduct industry-sponsored trials, cooperative group trials, and investigator-initiated clinical research studies from start-up to close-out.
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Based on a foundation of engineering and chemistry, Synthego leverages automation and machine learning to synthesize high-quality CRISPR reagents for science at scale. Experience executing process improvement or overseeing CAPA processes in a cGMP environment.
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Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials.
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Not available elsewhere, including clinical trials testing gene therapy for blood diseases like sickle cell disease ( Stem Cell Transplant and/ Pediatric Intensive Care Unit experience is preferred.
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trials job Title: wound care in Palo Alto, CA
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