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The Product Director must work closely with multiple functions including Sales, Sales Learning & Development, Commercial Insights & Strategy, Medical Affairs, Global Strategic Marketing, Communications, Regulatory, Health Care Compliance (HCC), Innovative Medicine affiliates, outside vendors and Key Opinion Leader speakers to effectively implement key commercial activities.
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The Product Director, Neuroscience Schizophrenia will lead Professional Education, Congress Strategy and KOL Engagement to build knowledge and skills associated with product and operational considerations.
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Work with CMC cross-functional teams and Regulatory Affairs teams. Requirements: BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5+ years in the pharmaceutical industry, preferably with 3+ years CMC regulatory experience, Sterile Injectable experience preferred.
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Work closely with individual clinical project teams as well as functional area partners in Regulatory Affairs, Market Access, Clinical Development, Epidemiology, Commercial Data Science, Translational Research, Statistics, and others.
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Experience in mortgage and consumer banking, whole loans, and asset-backed securities; capital markets, hedging, trading, pricing; securitization; and regulatory compliance. Ensures all activities are in accordance with company and regulatory risk and compliance requirements.
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Knowledge of Bank Secrecy Act regulatory requirements, including CTRs and SARs, and basic knowledge of banking regulations. BSA Analyst responsibilities include: Administering the Bank Secrecy Act/Anti-Money Laundering Program and related procedures in accordance with Bank’s policies, procedures, and applicable federal regulations.
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The Learning Experience Designer will apply instructional design principles, best practices, and creativity to develop a variety of learning resources to enable an industry-leading approach for training for Scientific Affairs and Medical Affairs.
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ERM delivers a wide range of climate change services including decarbonization strategy development, creation of Scope 1, 2, and 3 carbon inventories, Task Force on Climate-related Financial Disclosure (TCFD) analysis and reporting, strategy development, policy and regulatory analysis, target setting, and benchmarking.
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Demonstrated proficiency in interpreting gynecologic smears as required by regulatory agencies Essential Functions: Supervises cytology facet of laboratory. The department is closed for the following holidays: New Year's Day, Memorial Day, July 4th, Thanksgiving, and Christmas Day. Required Certifications: Certified ASCP Experience: 3 years of experience, including examination, interpretation, and classification of both gynecological and non-gynecological cytology specimens.
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Identify develop operational institutional pathways to grow scientific engagements research and data for the enterprise with a special focus on community oncology centers and accounts for ongoing working groups and consortium support Contributes to the scientific affairs HCE partnership execution with select external research partners to maximize effective and compliant delivery of research with external organizations.
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Develop and maintain data lineage documentation and mappings to support data governance, regulatory, compliance, and data lineage analysis activities. Strong understanding of data governance principles, data quality management concepts, and regulatory requirements (e.g. GDPR.
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Supports the overall management of and research required for regulatory exams, internal audits, and other monitoring and inspection reviews and evaluates data and information relevant to inspection metrics to support governance activities for dashboard reporting.
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As a Sr. Multimedia Design Specialist, you will need to be a web savvy graphic artist and digital video developer who has experience developing creative for digital marketing campaigns including website graphics, digital video and animation development, Adobe Experience Manager template and component designs, digital banner ads, HTML emails, PowerPoint presentations and slide development, as well as have a proficiency with marketing automation tools.
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Must understand regulatory servicing requirements including, but not limited to the Flood Disaster Protection Act (FDPA), Homeowner's Flood Insurance Affordability Act, Real Estate Settlement Procedures Act (RESPA), and Federal Rules of Bankruptcy Procedures.
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Stays up to date and compliant with the regulatory landscape related to drug safety and data analyses. The Associate will leverage a variety of analytics and visualization techniques to contribute to research, clinical development, drug safety and post-marketing activities.
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regulatory affairs jobs Title: sr associate in Trenton, NJ
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