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Serves as a subject matter expert in immunoassay-based assay development and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials.
$154,325 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Coordinates global CMC regulatory activities necessary to conduct clinical trials, achieve marketing approval of drug candidates and ultimately support the life-cycle of approved products.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Reporting directly to the Disease Team Project Manager, the Clinical Research Coordinator I is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
$51.44 an hourFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The Associate Director for Translational Research will partner with the AD of Clinical Science to prioritize clinical trials and partner with the AD for Community Outreach and Engagement to ensure that translational oncology initiatives are aligned with the MCC catchment area high priority cancer.
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Minimum of 5 years’ experience in clinical research, ideally as a SAS programmer for phase I-IV clinical trials in a pharmaceutical/CRO environment. Generate analysis datasets, tables, figures, and listings to support the statistical analysis of clinical trials data in support of regulatory submissions and publications under supervision of biostatisticians.
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Working with a team of interdisciplinary data scientists, engineers, architects, and consultants, our work includes novel areas such as cancer detection, drug discovery, optimizing population health and clinical trials, autonomous systems and edge AI, and renewable energy.
$218,625 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Clinical Development Lead will be responsible for leading the design of clinical trials and the development of protocols to meet the CDP objectives and for contributing to key regulatory documents and study level documents including the review and dissemination of study results and related publications.
$386,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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These include specific Abzena capabilities such as mammalian biologics development and manufacture of material for clinical trials through Phase III and small-scale commercial manufacturing.
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Ph. D in Statistics, Biostatistics or related discipline with 15 or more years of experience leading biostatistics function for phase I-IV clinical trials in biotech, pharmaceutical industry and/or CRO environment.
$325,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Knowledge of HIV research, including knowledge of HIV disease and treatments with experience in operation and management of clinical trials or studies. DESCRIPTION The UCSD Mother-Child-Adolescent Program (MCAP) has been providing comprehensive and integrated HIV care, social services, and clinical research to women, infants, children, and youth ages 13-24 for over 30 years.
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HJF is seeking a Pathologists Assistant III the incumbent will be responsible for performing biospecimen collection in support of multiple Murtha Cancer Center Research Program (MCCRP) research protocols at Naval Medical Center San Diego (NMCSD) in San Diego, CA to help expand the MCC biorepository throughout the MHS‐wide Military Clinical Trials Network.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The Director, Clinical Data Management will be responsible for daily data management tasks for all phases of clinical trials including CRO oversight and support other functional areas such as clinical operations, statistical programming, biostatistics, and medical monitor.
$242,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Work with key internal and external stakeholders to lead the design and implementation of the CDP and the design of clinical trials to meet the objectives of the CDP. In depth knowledge of drug development process and oversight of clinical trials.
$386,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Under the supervision of the Site Director, the Detox Technician will be responsible for supporting various activities associated with the day-to-day operations of the research department in the conduct of clinical trials in psychiatry and internal medicine.
$22 - $25 an hourExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Leading the legal support for supply chain, clinical trials and regulatory issues, evolving to support commercialization capabilities. 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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clinical trials jobs in San Diego, CA
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