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This remote opportunity involves working predominantly during first shift hours (7 am - 4 pm CST), with some flexibility to accommodate European time zones.
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The Clinical Operations Specialist provides operational support as the subject matter expert for business applications, systems and tracking to initiate and execute contracts and to process payments for Clinical Research & Operations as well as Scientific Data & Communications.
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The Technical Writer and Document Specialist (TW/DS) will sit within the Cell Therapy Development (CTD) Development Operations and Services (DO&S) Portfolio Management Office (PMO). This individual will be responsible for delivering CMC documentation (Dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application.
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Specialized experience is defined and experience which includes monitoring Communications Security (COMSEC) activities AND applying logistical support policies, procedures, and/or guidance regarding Information Assurance (IA) equipment or systems.
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Sales Support, Clinical Specialist - Peripheral, Image - Guided Therapy Devices (Central New Jersey)
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Sales Support, Clinical Specialist - Peripheral, Image-Guided Therapy Devices (Central New Jersey) Provides ongoing support for company-sponsored clinical/marketing trials and registries.
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Blue Star Architectural Glass, Inc. ("The Company") is currently seeking an experienced Accounts Payable Specialist to support our rapidly growing construction business. Provide audit support.
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Whitestone Associates, Inc., a 100% employee-owned company and leading provider of environmental and geotechnical engineering and consulting services throughout the eastern US, is currently recruiting for an HR Technology Specialist to join our Warren NJ office.
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Reporting to the Supervisor of the Cellular Services Lab, the Senior Lab Specialist will perform multiple processes including PBMC isolation and cryopreservation, other assays, and tests; propagates non-animal specimens and cell cultures; prepares biomaterials including stool for testing.
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The Regulatory Specialist Raw Materials is to support the Regulatory Team, and to keep current with industry regulations, providing interpretations for the completion of internal and external customer requests.
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Support and implement continuous process improvement ideas and initiatives. Initial draft authoring of scientific content for Common Technical Document (CTD) Quality sections and responses to health authority questions aligned with regulatory strategy for cell therapy clinical CMC regulatory submissions based on high quality technical reports.
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Managing Risk - Assessing and effectively managing all of the risks associated with their business objectives and activities to ensure they adhere to and support PNC's Enterprise Risk Management Framework.
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As a sustainable company, we give new life to pieces by thousands of brands across numerous categories—including women's and men's fashion, fine jewelry and watches, art and home—in support of the circular economy.
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This role manages all workflows related to PVAs in the region in collaboration with the regional business, Patient Safety, and other functions, as well as the process requirements for registering all patient support and market research programs (PSP/MRP) with GPS in the region.
$45 an hourFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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This individual will be responsible for delivering CMC documentation (Dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from an early stage through registrational application.
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Expertise in embankment dams and levees, flood protection facility design, foundation design (deep and shallow), excavation support systems, dewatering, pipeline work, and solid waste. Serve as a technical specialist in the application of advanced geotechnical engineering theories, concepts, principles, and processes for wide range in multidisciplinary projects.
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