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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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Participate in the I-SPY TRIALS, a ground-breaking national public-private collaboration among NCI, FDA, more than 20 cancer research centers, and major pharma, biotech companies as well as the University of California-wide Athena Breast Health Network, a learning system designed to integrate clinical care and research as it follows 150,000 women from screening through treatment and outcomes.
$250,000 - $360,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are seeking a Senior Clinical Trial Specialist to assist in the execution of Clinical Trials. The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and HI-Bios SOPs. The Specialist provides a high level of administration, coordination and organizational support to the Clinical Study Lead and team members from all functions involved in assigned study(ies.
ExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Some understanding of FDA regulatory processes and clinical trials is preferred. This position will partner with functional sub-team leaders to lead project management activities for a cell therapy program sub-team, guiding the sub-team through preclinical and clinical development.
$145,000 - $175,000 a yearFull-timeExpandUpdated 13 days ago - UpvoteDownvoteShare Job
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Oversee the CRO development of SAS programs for the creation of SDTM and ADaM data sets following CDISC standards for OED clinical trials and allowing for integrated data at AbbVie. Oversee the CRO development of SAS programs for the creation of Tables, Listings and Figures for OED clinical trials.
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Carbon Health is looking for an excellent full-time Primary Care Physician with clinical research experience as a Principal Investigator to join a growing community of healthcare providers to deliver compassionate, evidence-based urgent care and conduct clinical trials in infectious disease and indications related to general medicine, including vaccine research and cardiometabolic health.
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We have built a deep portfolio of AVV-based gene therapy product candidates, with five product candidates in clinical trials: 4D-150 for the treatment of wet age-related macular degeneration (wet AMD) and diabetic macular edema (DME), 4D-710 for the treatment of cystic fibrosis lung disease, 4D-310 for the treatment of Fabry disease cardiomyopathy, 4D-125 for the treatment of X-linked retinitis pigmentosa (XLRP), and 4D-110 for the treatment of choroideremia.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Minimum of 5 years’ pharmaceutical industry drug safety experience, optimally in a small-to-mid cap biotech environment Global clinical trials experience ex-North America in one of either EMEA or APAC strongly preferred.
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As a CTM, you will be responsible for planning and managing our early development clinical trials in kidney disease while ensuring high quality data and timely clinical trial conduct per GCP standards.
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Reviews sections of IND/CTA, BLA/MAA, and other global submission documents in support of clinical trials and marketing applications, and their amendments in conformance with local regulatory requirements.
$251,000 - $385,000 a yearFull-timeExpandUpdated 13 days ago - UpvoteDownvoteShare Job
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The Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.
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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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Enrollment of patients on national clinical trials (SWOG, ECOG, NRG, NCI), developing regional practice care pathways, enhancing the reputation of our program via Commission on Cancer accreditation projects, participating in clinical research projects and other opportunities to enhance ones' practice are available in our program.
$385,080 - $400,020 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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As part of a growing clinical development operations team, the Specialist will help define various aspects of clinical trials to ensure timely completion, efficient protocols, budget alignment, and compliance with ICH/GCP Guidelines.
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clinical trials jobs in San Francisco, CA
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