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Knowledge and understanding of the various laws, regulations and industry guidance including, but not limited to, transactional matters (e.g., drafting, reviewing and negotiating corporate, commercial and procurement contracts), fraud and abuse (e.g., Anti-Kickback Statute, False Claims Act, Anti-Trust), FDA regulatory matters, and general corporate governance.
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Ensure that all activities and duties are carried out in full compliance with regulatory requirements, Enterprise Wide Risk Management Framework and internal Policies and Policy Standards. The environment we operate within is continually changing and Operations plays a key role in driving market initiatives and regulatory changes.
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Provide counsel on corporate, commercial, and regulatory matters, employment law, litigation, and risk management, with a focus on contracts, intellectual property, and compliance. Stay updated on regulatory developments in product liability, data privacy, and international trade as they relate to IoT and audio technology.
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Profile: A law firm is seeking a Securities Litigation Associate Attorney to join their team in Florham Park, NJ. The ideal candidate will have 4-6 years of substantive experience in securities litigation and regulatory practice, working on a variety of matters, including arbitrations, regulatory enforcement actions, and compliance issues.
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Maintain a safe work environment and wear appropriate personal protective equipment Qualifications: Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements.
$60 - $76.92 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Bressler, Amery & Ross, a dynamic and growing national law firm, seeks a Securities Litigation & Regulatory Associate Attorney to join our Financial Institutions Practice Group located in our Florham Park, NJ office.
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Experience in the testing of control methodologies within a financial institution including control monitoring, control evaluations and measurement of control effectiveness in accordance with regulatory compliance requirements such as corporate governance, consumer protection, AML/CTF and Financial Crimes, data protection/data privacy, ethics or conduct risk.
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Thorough understanding of heterogeneous customer needs including Medical scientific fora, Regulatory Authorities, Health Technology Assessment bodies and major national payers; The RWE Lead will lead a cross functional team for the development of integrated evidence generation plans across the entire product life cycle with the mandate serving research, development, regulatory, medical, and commercial strategies and needs.
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Job Title: Regulatory Studio - Associate Director, Precision Medicine & Digital Health. Kept up to date on Digital Health technology regulatory requirements and worked on a digital pathology or digital health product in a drug.
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Maintains knowledge of Federal, State, and other regulatory agency rules and regulations including The Joint Commission, CMS, Medicare, including but not limited to, knowledge of CMS rules regarding Observation status, the 2 Midnight Rule, and Medicare Inpatient Only Procedures.
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Support Sr. Director, Supply Chain on new projects with existing partners, collaborate with Business Development, Product Development, Supply Chain and Regulatory, for developing the right business model complementing the partner capabilities.
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The Validation Specialist will play a key role in ensuring that all processes, systems, and equipment within the client organization are commissioned, qualified, and validated in compliance with regulatory requirements and industry standards.
$50 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Principal Scientist will work closely with individuals from Clinical Research, Regulatory Affairs, Biostatistics, Outcomes Research, and Operations to ensure COA endpoint strategies are consistent with and executed and interpreted to support the product strategy.
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Partner with Drug Metabolism and Pharmacokinetic (DMPK) and Bioanalytical (BA) Subject Matter Experts (SMEs) to author, review and track regulatory documents. Understand the impact of DMPK/BA and interdependencies with other functional teams within the enterprise including Pharmacology, Toxicology, Clinical and Regulatory disciplines.
$59 an hourFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic tests, digital health and other devices to enhance the value of our pharmaceutical products across therapeutic areas.
ExpandApply NowActive JobUpdated 18 days ago
regulatory job Company: Taco Bell in Summit, NJ
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