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Clinical Stage Biotechnology company is hiring a Director, Downstream Process Development to help advance the organization's lead program to commercial launch. Lead the Process Development group to develop globally compliant, robust, well-characterized, scalable and high quality AAV production platform to support both internal and external (CDMO) manufacturing requirements for clinical and commercial programs.
$225,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Executive Director, Global Clinical Supply Chain - Virology United States - California - Foster City Manufacturing Operations & Supply Chain Regular. Executive Director, Global Clinical Supply Chain (GCSC) - Virology.
$355,410 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The C3 AI Platform supports the value chain in any industry with prebuilt, configurable, high-value AI applications for reliability, fraud detection, sensor network health, supply network optimization, energy management, anti-money laundering, and customer engagement.
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Gilead is hiring an Associate Director level experienced, well-organized professional, who will develop, implement, and manage the strategic publication plans for global clinical studies and non-clinical sources, including HEOR, Epidemiology, RWE, Payer, Non-interventional, and database studies, to demonstrate the value of pipeline and inline products in Liver Hepatitis.
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Conduct drills and trainings for building staff and tenant floor wardens in accordance with California Title 19 Code of Regulations and maintains High-Rise Fire Safety Director License. Work with Director of Leasing on preparing vacant spaces for leasing, overall marketing strategy and building positioning.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Bachelor's degree in Mechanical Engineering, Materials Science, Supply Chain Management, or a related field. Minimum of 5 years of experience in supply chain management, preferably in the consumer electronics industry.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Transfer Pricing (TP) competency addresses planning, documentation and controversy issues associated with all types of intercompany transactions, assisting companies with supply chain matters, with a focus on intangible property and helping companies accurately reflect and monitor their transfer pricing in their financial systems.
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As the Assistant Director, Gift Administration reporting to the Director of Gift Accounting and Fund Management, you are primarily responsible for managing gift processing operations, planning and implementing gift-related projects and process development, and managing a team of up to three Gift and Data Processing Specialists.
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The Assistant Program Director will have documented expertise in nutrition and/or pediatric research, including clinical trials research experience. Experience with nutrition research, community partnered research, clinical trials research, mixed methods research, and ability to communicate well with community partners, researchers, funders, and philanthropists.
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Represent QC in cross-functional teams (Analytical Development, QA, Manufacturing, Product Management, Supply Chain departments) to meet product release timeline and manage stability programs to ensure timely testing, real time trending and generation of stability reports.
$220,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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At Ivalua we are a global community of exceptional professionals, who believe that digital transformation revolutionizes supply chain sustainability and resiliency to unlock the power of supplier collaboration.
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In addition to the main campus, the hospital maintains four clinical locations and a Life Flight facility. Oncology nurse, oncology, cancer treatment, cancer RN, cancer care, patient care, RN, R.N., healthcare, health care, nursing, nurse, onc, onc RN, oncology RN, medical, hospital, outpatient American Mobile Healthcare Job ID #3139896.
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Oversee and provide strategic direction for Toxicology/Pathology, BioAnalytical/DMPK, Biomarkers, and Clinical Pharmacology teams to ensure robust support for clinical development programs.
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Manage and maintain the Trial Master File (TMF) throughout the lifecycle of clinical trials, including. This role involves managing TMF systems, process oversight and optimization, and supporting the inspection readiness of clinical trials in adherence to the requirements of study protocols.
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Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials.
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clinical trials director supply chain jobs in San Carlos, CA
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