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Perform analysis, interpret study results, and collaborate with clinical team to conduct interim data review, final reports, and publications. Arcellx isa public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases.
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Today, our team consists of creators and communicators with varied backgrounds - from Stanford, to the Indian Institute of Technology, big companies and one-person startups, the United States, and abroad.
$119,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Solid understanding of relevant FDA, EU, and ICH regulatory guidelines and pharmacopeia as applicable to stability study design, expiry dating, and analytical method qualification/validation for biologics and vaccines.
$144,000 - $162,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The Volunteer for International Experience (VIE) program is an international program sponsored by the French Ministry of Economy, Finance and Employment, open to Airbus to offer young professionals the opportunity to have valuable paid work experience abroad in a technical or business function.
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Study Epidemiologist HIV) Draft and review observational study analysis specifications, including statistical analysis plans (SAPs) Review analysis outputs for quality, including study analysis, ad hoc analysis, analysis to support conference or publications.
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Candidates will likely have a background in clinical research, knowledge of research coordinator responsibilities and the pre-award and post-award operational and financial aspects of study management, and experience or a desire to develop as a presenter and trainer.
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Work with product, regulatory, privacy, security, engineering, operations, sales, and marketing teams to develop strategy for various market segments and verticals in U.S. and abroad (including financial services, heathcare, SLED, and public sector.
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Translates trends in operational and systematic issues and develops solutions with sustainability in mind to ensure roadblocks are removed during study start-up. Triages study-level vendor management issues; escalates high-risk issues to appropriate stakeholders.
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Write and review SOPs related to DDCPE activities, ensuring alignment with other company SOPs. Design and write packaging study protocols and reports that support product development and regulatory filing needs.
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Hands-on design of clinical trials, including selecting appropriate study designs, endpoints, and patient populations to facilitate adoption, regulatory approval and/or reimbursement of the Karius Test for infectious disease indications.
$240,000 - $310,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Requires an BA/BS degree in Information Technology, Computer Science or related field of study and a minimum of 6 years experience in audit (information technology, operations or financial), desktop (MS Office-Excel, Word, Access, Project), audit and regulatory requirements and standards (PCAOB, CobiT, SAS70, SOX etc.
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10 years or more of experience in pharmaceutical clinical drug development in industry including protocol development; study initiation and follow-up; IRB/EC submissions and interactions; review of clinical study data listings; review and/or preparation of clinical study reports.
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Knowledge, Experience, and Skills:Minimum of a Master’s degree in Biomedical Engineering, Mechanical Engineering or related field of study and 4+ years of relevant experience; or Bachelor's degree and 6+ years of relevant experience.
$133,280 - $172,480 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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This position will report directly to a Director of Biostatistics, and will be tasked with the study deisgn, analysis, and submission of multiple trials and indications in various TA's - an excellent opportunity for a Senior Manager looking to gain experience.
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Study takes two years full time, or three years part time, and must be followed by registration with the HPC before official practice can start. Art therapists need a postgraduate diploma in art therapy or psychotherapy that is recognised by the Health Professions Council Course providers often require candidates to hold degrees in art-based subjects, although relevant qualifications such as nursing, teaching or social work may be accepted.
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study abroad jobs in Belmont, CA
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