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Lead CMC regulatory activities in the late development and/or lifecycle management of GSK products. Ensure all appropriate CMC regulatory aspects for product release are in place, to ensure continuity of market supply.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The Regulatory Affairs Professionals Society (RAPS) is the largest global organization of professionals involved with regulatory and quality for healthcare products, including medical devices, pharmaceuticals and biologics, diagnostics, and digital health.
$72,800 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Provide expert legal guidance and strategic advice to the General Counsel, executive leadership team, and various business units on a broad range of legal matters, including contract law, regulatory compliance, litigation, employment law, and commercial transactions.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Analytical Development, Vaccine Development, GMP, quality control, compliance, investigation and analysis, method validation, method transfer, regulatory filing, Large Molecule, analytical method, regulatory standard, glp, validation protocol, analytical methods, release, stability, in-process assays, technical liaison, deviations, investigations, drug development, ICH, CMC guidance documents.
ExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Strong understanding of pharmacokinetics, biomarkers, statistical principles, and regulatory requirements and demonstrated experience integrating these disciplines in the context of drug development.
$342,410 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Collaborate across Process Development, Quality, Supply Chain, Manufacturing, CMC Regulatory Affairs, Finance and Technical Development for successful commercialization of late-stage portfolio.
$328,900 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Work closely with Regulatory Operations to ensure on-time submission of required documents. Advanced degree in pharmacy, regulatory affairs, nursing or other life science is preferred. Provide critical regulatory review of promotional and non-promotional external communications.
Full-timeRemoteExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have solid experience in nuclear power plant design and regulatory requirements and will be capable of developing licensing and design documents that maintain safety in design.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Participate in on-site audits of registered duties, documentation, and processes in order to comply with Navy Federal standards and FINRA, NASAA, SEC and other regulatory agencies. Provide basic investment consultation related to investment products, life insurance services and related quotes, document preparation and required regulatory filings.
$75,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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The Archaeology Program Manager will have extensive knowledge of archaeology data collection methods, data analysis, and data interpretation, demonstrated knowledge of the regulatory environment, high-level technical writing skills, and the ability to direct and mentor staff.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This includes providing technical consulting on a wide range of engineering and regulatory projects in addition to supporting day-to-day nuclear power plant operations. The consulting engineer's functions as part of a corporate risk management team that interfaces with multiple nuclear plant departments to implement the risk management (PRA) program.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Maintain and update files of all applicable regulatory documentation for Institutional Review Board (IRB). Instruct data entry and clinical staff in procedures relative to data management, protocol instructions, Standard Operating Procedures and regulatory processes and considerations.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Assist in the preparation and review of bioanalytical data and reports suitable for regulatory submission. Background in molecular biology techniques such as cloning, site-directed mutagenesis, DNA and RNA isolation and purification, sequencing, RT-PCR, and qPCR.
ExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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They possess deep expertise in designing and interpreting real-world evidence studies using advanced statistical methods and various data sources, coupled with a thorough understanding of regulatory guidelines.
Full-timeExpandApply NowActive JobUpdated 1 month ago
regulatory job in Potomac, MD
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