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We are looking for a Quality Assurance Analyst with a solid interest in human anatomy to help us build the digital twin platform. Q Bio was founded in 2015 by serial entrepreneur Jeffrey Kaditz, Dr. Michael Snyder, Chair of Genetics and Director of Personalized Medicine at Stanford University, and Dr. Garry Choy, physician, radiologist, and former Chief Medical Information Officer at Mass General Hospital.
$75,000 - $80,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Associate Director of Clinical Quality Assurance will be responsible for building the clinical quality assurance processes and providing quality oversight for the clinical programs and CRO throughout the development stages of antibody-based radiopharmaceuticals.
$155,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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You will develop and provide training to teams in performing clinical functions that meet statutory, regulatory, and contractual requirements for the services provided and meet PTC (Pinnacle Treatment Center) clinical quality expectations.
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The Associate Director will work closely with colleagues in Clinical Regulatory, Quality, Technical Operations, and Translational Medicine both as a leader and as an individual contributor for the development of effective product development strategies.
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Description : Under the supervision of the Program Director, the Trainee/Clinician provides clinical and rehabilitation services to adults with psychiatric disabilities living in or in transition to the community in San Mateo County.
$31 - $37 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform quality assurance review and approval of investigation, deviations, OOSs/OOTs, Change Controls, CAPAs and. Create product quality documentation system by writing and updating quality assurance procedures.
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Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.
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Maintains records of the quality assurance testing so that easy reference is available should servicing be necessary. Assists quality assurance technicians in performing quality assurance testing on the equipment using phantoms, test tools, test check lists, etc.
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Responsibilities and duties of each role engaged in any phase of testing are clearly defined in writing, identifying which examinations each role is authorized to perform, whether supervision is required, and whether supervisory or Clinical Laboratory Medical Director review is required before reporting test results.
$340,000 - $460,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the Associate Dean and Karr Family Director of the Black Community Services Center and working alongside the Associate Director and Assistant Director, the Project Pipeline Project Manager of the Black Community Services Center (BCSC) is an administrator that comprises the career staff in the center.
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The Associate Director, Clinical Records & Information Management will partner with cross functional teams as well as Clinical Research Organization (CRO and Functional Service Provider (FSP) to ensure timely and quality delivery of the TMF. This role is a member of the Clinical Records leadership team to ensure optimum implementation of the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program.
$191,335 - $247,610 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provide Statistical leadership to Virology clinical trials: developing trial design options and providing high quality decision support. The Associate Director will be primarily responsible for the business, operational, and compliance aspects of Virology drug discovery, development, and marketed products at Gilead.
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The Program Associate Director serves as student advisor on impact pathways, acts as the Center's liaison with the Marketing department for external communications and has project management, representation, and oversight responsibility for all aspects of the GSB Impact Fund's business.
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NPM is looking for an experienced Director, AI Data Scientist / Machine Learning Engineer to join our dynamic team and drive innovation to extract, synthesize, and analyze information from unstructured clinical notes.
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Reports to: Director, Protein Development and Clinical Manufacturing Location: San Carlos, CA Compensation: The compensation package will be competitive and includes comprehensive benefits and an equity component.
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director clinical quality assurance cqa jobs in Redwood City, CA
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