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The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.
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Excellent understanding of the business processes, GCP standards and software used in clinical trials, outcomes research and real-world evidence generation. We are seeking an exceptional Senior Principal Statistician with strong statistical and computational skills to support multiple complex clinical trials in Oncology and COVID. The Senior Principal Statistician is responsible for leading and performing biostatistics and statistical programming activities in these trials, which may be Phase I, II and III pharmaceutical trials and medical device trials evaluating new biomarkers and/or therapeutics.
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The Community Practice Clinical Data Coordinator at Trial Library will play an integral part in expanding access to cancer clinical trials by pioneering pre-screening efforts in community oncology settings.
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The trials also involve real world evidence generation, patient reported outcomes (PROs) and analysis of complex big data sets. Quantum Leap Healthcare Collaborative (QLHC) is seeking an exceptional Data Scientist with strong analytical and computational skills to support multiple complex clinical trials in Oncology and COVID. The Data Scientist is responsible for performing data analytical and programming activities in these trials, which may be Phase I, II and III pharmaceutical trials and medical device trials evaluating new biomarkers and/or therapeutics.
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Experience with clinical trials regulatory affairs, or related clinical trials experience such clinical research coordinator experience. Review, provide feedback, and approve Medicare coverage analysis and budgets for complex clinical trials; serve as point person from study team for budget negotiations.
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Licensure for management, healthcare and/or clinical trials coordination (i.e. PMP, CCRP, SoCRA). Assist PI with the development of concept sheets, protocols, investigational brochure or package insert, and consent forms working in close collaboration with the Protocol Development team for investigator-initiated trials.
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Knowledge in breast imaging acquisition methods (MRI, mammography, ultrasound and/or PET) and clinical trials is highly desirable. The Department of Radiology and Biomedical Imaging at UCSF is seeking a postdoctoral fellow interested in quantitative imaging and data science with application to breast cancer diagnosis and treatment.
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The successful candidate will work closely with the translational sciences and clinical operations teams to ensure the successful integration of novel biomarker assays into clinical trials in pulmonary fibrosis, biliary fibrosis, oncology, and muscular dystrophy.
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Work closely and collaboratively with the Clinical Operations team to ensure successful application of biomarker/pharmacodynamic assays in clinical trials (e.g. provide assistance with clinical document writing/review, sample logistics, data transfers, data interpretation, etc.
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The Associate Director of Quantitative Science is a self-sufficient and high-impact position that focuses on supporting the statistical and data science needs in the risk-based monitoring (RBM) of clinical trials, serving in roles such as CSM lead (CSM: Centralized Statistical Monitoring), while also support other activities such as preclinical studies, biomarkers, application of AI/ML and development of analysis applications.
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Work with statisticians/biometrics to develop the required tables/listings/figures and contribute to the interpretation of efficacy and safety data from clinical trials. This person will provide scientific and clinical expertise to develop, design, conduct, analyze, and report global clinical trials in accordance with approved clinical development plans and Health Authority (e.g., FDA/EMA, etc.
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Broad knowledge of commercial disputes and experience setting case strategy, managing discovery process, and managing mediation/arbitration and trials. You will help to develop and implement proactive policies to ensure compliance with global laws and regulations in different subject areas, including intellectual property, anti-corruption, competition, revenue-recognition, records retention, privacy, and data security.
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Ensure that CRO/CMO activities and other process development activities address drug substance needs for pharmaceutical formulation development, toxicology testing, clinical trials, and commercial launch.
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Explore novel statistical approaches through which real-world evidence can be used as a supplement to interventional trials. Expertise in analytic languages (e.g. python, R, SQL, SAS); R or python is preferred, but we welcome applicants who are willing to learn and use either.
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We’re seeking an experienced Senior Clinical Research Associate to join the Veterinary Operations team that achieves its mission through developing veterinary partnerships, engaging with the veterinary community through education, ensuring excellence in the science behind our products, executing clinical trials and studies.
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trials job in San Francisco, CA
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