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As an industry leader, ArisGlobal offers software as a service for Clinical Trials, Regulatory Affairs, Drug Safety, and Medical Affairs. As an industry leader, ArisGlobal offers software as a service for Clinical Trials, Regulatory Affairs, Drug Safety, and Medical Affairs.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Act as a liaison between cross-functional teams, including clinical operations, regulatory affairs, finance, and business development, fostering strong communication and collaboration throughout the contract lifecycle.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Partner with Engineering, Quality, Manufacturing, CM/OEM, Marketing, Regulatory Affairs, and other key functions to achieve business goals. Job Title - Principal Electrical Engineer. Demonstrated capability/understanding of the design and development of medical devices including electro-mechanical assemblies, mechanisms, metal and plastic components, and manufacturing processes.
ExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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8+ years of regulatory affairs experience in drug development and product registration activities within the pharmaceutical or biotech industry in multiple phases of development; both big and small company experience is preferred.
ExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Proclinical is seeking a Director, Regulatory Affairs for a mid-sized oncology focused biotechnology company with their site in Massachusetts. Report to our Head of Regulatory Affairs and work side by side with your R&D colleagues to develop and execute innovative regulatory strategies for their development programs (from FIH through late-stage clinical programs), including the implementation of non-clinical and clinical regulatory strategy for relevant products.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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As the RC Regulatory Affairs representative, work with brands on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies, and applicable Industry Guidelines for the advertising and promotion of prescription drugs, biologics, and devices.
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Minimum of 3-5 years of experience in regulatory affairs, compliance, or a related field within a healthcare setting. Experience with Joint Commission accreditation processes and standards, or regulatory compliance experience.
ExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Our advertising agency client is looking for a Medical Editor with 5+ years' experience for an immediate contract going until end of year; you'll be working on editing, proofing and fact checking medical information as well as medical affairs content.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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At least 5 years of relevant experience in medical devices regulatory affairs. Review and provide strategic regulatory input on product and package labeling as required. Provide ongoing support to cross-functional teams, offering regulatory strategies during product development.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Minimum of 6 years of regulatory affairs experience in the biopharmaceutical industry, with a focus on rare diseases and orphan drug development. Provides support to regulatory affairs reviewers for due diligence initiatives, including opportunity and risk assessment.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Contribute towards the overall Department Regulatory Affairs and Compliance infrastructure at CCA. Promote compliance in CCA’s business operations with all Medicare and Medicaid contractual and regulatory requirements.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Takeda Development Center Americas, Inc. is seeking a Director, PV Risk Management in Cambridge, MA with the following requirements: Master's degree in Regulatory Affairs, Pharmaceutical Sciences, Public Health, or life sciences or related field or foreign academic equivalent plus 8 years related experience.
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Providing advice on regulatory issues for both marketed and pipeline products; actively collaborates with management, Global Regulatory Lead and cross functional colleagues within Alexion (i.e., commercial, research, clinical development, medical affairs, business development, legal, manufacturing, quality, portfolio management, financial, human resources, etc.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Contributes to the inspection readiness program and acts as subject matter expert (SME) on pharmacovigilance operations in regulatory inspections and company audits including FDA/MHRA/EMA PV inspections as needed.
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Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program leadership and develop CMC regulatory strategy for global vaccine programs in various stages of development.
$266,200 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago
regulatory affairs jobs in Boston, WA, Ohio
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