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Author, and approve protocol and reports in accordance with internal and external regulatory expectations (APS, Engineering, Tech Transfer). Author, and approve protocol and reports in accordance with internal and external regulatory expectations (APS, Engineering, Tech Transfer.
$60 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Offer user support and feedback on references and core claims library within the Medical/Legal/Regulatory review and approval system (Veeva Vault PromoMats) Maintain reference and claims library relevancy, working with Medical/Regulatory, conduct periodic audits of the information on file.
$45 - $48 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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As the driving force behind our compliance and risk management framework, you’ll work closely with the Chief Compliance Officer to shape the future of our regulatory landscape. Regulatory Engagement: Assist the CCO in navigating regulatory inquiries, examinations, and internal audits.
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Its lawyers provide litigation and other dispute resolution services in multi-jurisdictional and other high-stakes matters; deliver regulatory counsel; and execute the full range of strategic domestic and cross-border transactions.
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This role will focus on setup, maintenance, and management of a global centralized library of references to support the creation of content and the submission of materials for Medical, Legal and Regulatory review and approval.
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Performs tech transfer facility fitness, gap analysis, and risk assessment when on-boarding new programs. Familiarity with cell therapy processes and cGMP is strongly preferred. Minimum 3 years relevant experience in GMP biologic/cell therapy manufacturing technical or process support.
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Conduct thorough review and collection of AML/KYC documentation to ensure compliance with regulatory standards. Summary: The AML & KYC Analyst plays a critical role in our organization by ensuring adherence to anti-money laundering (AML) and Know Your Customer (KYC) regulations.
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The Software Engineering Manager will work on business and regulatory requirements related to various regulations like CECL. The role requires subject matter expertise in Asset Liability Management at Financial Institutions along with proficiency in financial modeling as well as tools and methodologies used for business analytics.
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Applicants must possess a current and valid license as a Speech Pathologist/Audiologist issued by the Audiology and Speech-Language Pathology Advisory Committee, Division of Consumer Affairs, Department of Law and Public Safety.
$72,014.33 - $949,416 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Global Financial Crime (“GFC”) Executive - Global Wealth and Investment Management "GWIM" contributes to the direction and drives the development of enterprise-wide money laundering, economic sanctions, and fraud compliance and operational risk practices consistent with applicable laws, rules, regulations and regulatory guidance.
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Managers of Statistical programming provide comprehensive programming expertise to clinical project teams to support the development, regulatory approval and market acceptance of Bristol Myers Squibb (BMS) products.
$158,496 - $173,326 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Programmer with ETL experience specially with background in Python, regulatory projects, Capital , FRTB, SACCR. Experience of Alteryx like tools and who has prior exp in reporting/dashboard prototypes (may be using tableau) specially around capital reporting.
$110,000 - $115,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Author, and approve protocol and reports in accordance with internal and external regulatory expectations (Client, Engineering, Tech Transfer)." Author, and approve protocol and reports in accordance with internal and external regulatory expectations (Client, Engineering, Tech Transfer.
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Description/Comment: - ONSITE POSITION - DURATION - MINIMUM MONTHS AND MAY BE TEMP TO HIRE FOR RIGHT CANDIDATE - SHIFT - MON-FRI AM TO PM - MUST HAVE - GENE/CELL THERAPY MANUFACTURING EXP. The MS&T Specialist provides technical support to Princeton, NJ Facility.
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Offer user support, feedback, and answer questions about references and core claims library within the Medical/Legal/Regulatory review and approval system (Veeva Vault PromoMats) This role will focus on setting up, maintaining, and managing a global centralized library of references to support content creation and submitting materials for Medical, Legal, and Regulatory review and approval.
Full-timeExpandApply NowActive JobUpdated 4 days ago
regulatory affairs jobs Title: sr affairs associate Company: Thermo Fisher Scientific in Lawrence, NJ
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