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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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Adapt data science algorithms (supervised and unsupervised learning, decision trees, neural networks, AI based image processing and feature extraction, Bayesian learning, etc) for modeling clinical trial data to support drug development.
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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. 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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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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Ensure that the Trial Master File (TMF) is maintained and up to date. Ensure that clinical trials are executed according to the Clinical Development Plan (CDP), trial plans, OGSM and in compliance with argenx procedures, ICH-GCP and other applicable legislations.
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As a Senior Trial Attorney, you’ll represent clients under both commercial and personal lines insurance policies independently as lead counsel, as well as be part of a larger team as needed. This position will be a remote work from home opportunity reporting into our Sacramento, CA Trial Division office.
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Preferred Qualifications At least one year of previous experience as a clinical research coordinator or equivalent combination of experience / training Fluent in spoken and written Spanish and/or Arabic About UCSF The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.
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The candidate will be accountable for clinical trial study start up, maintenance, and close out. 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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You will lead internal peptide therapeutics development projects from drug discovery to Phase-2 clinical trials. PhD, MD, DO, DVM, or equivalent in Chemistry, Biochemistry, Medicinal Chemistry, or related field.
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Responsible for ensuring that allcomponents of the trial master file (TMF/eTMF) are up-to-date and accurate for QED-assigned investigational trials. Knowledge of GDPR and how to apply appropriate practices to clinical trials.
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Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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Proficiency in (or willingness to learn) instructional and other technology, such as: Learning Management Systems (Canvas); lecture/presentation capture applications (Panopto); online video conferencing (Zoom); Microsoft Office (Word and PowerPoint); file sharing (Google drive or Dropbox); and Google Workspace tools (email, calendar, docs, sheets, slides, etc.
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Licensed Master Social Worker (LMSW) Licensed Clinical Social Worker (LCSW) Licensed Clinical Social Worker Psychotherapy (LCSW-R) Licensed Professional Clinical Counselor (LPCC.
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We are using models early to fail less often, executing clinical trials to add valuation to the company, and generating fit-for-purpose data to feed back into Valo’s Opal Computational Platform as we reinvent drug discovery and development from the ground up.
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THE ROLE: Temporary Master Data and Implementation Specialist The Temporary Master Data and Implementation Specialist role is responsible for the accuracy, integrity, and timeliness of master data in OLLY's ERP system Microsoft Navision.
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clinical trials trial master file jobs Title: trial master file in San Francisco, CA
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