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First line operations manager of all activities at MercyOne Des Moines and a member of the pharmacy leadership team. This manager will have direct management of pharmacists, pharmacy technicians, and other support staff providing pharmaceutical care to patients of all ages including neonatal, infant, pediatric, adolescent, adult, and geriatric with the assistance of manager of technicians, clinical pharmacy manager and Market Director.
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As an integral member of Pharmacy Services, the IDS/Pharmacy Regulatory Coordinator's role also includes assuring accurate record keeping, filling, compounding and delivering of investigational drug products to study coordinators, study nurses and patients.
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Analytics Insights, Business, Business Direction, Client Relationship Management, Finance, Global Market, Marketing Strategies, Portfolio Management, Regulatory Compliance, Sales, Structured Products.
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Work with Senior regulatory personnel / Manager to identify regulatory and product registration needs and requirements for new products. Responsibilities: The Snr Product Regulatory Specialist is responsible for obtaining registrations and certification approvals for new and existing products, necessary to sell them to worldwide markets.
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Highly reputable, established, Fintech looking to appoint a Legal Counsel/ Financial Services Regulatory Counsel in NYC to expand their In-House legal and regulatory compliance capability/ team.
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The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS), Company Core Safety Information (CCSI) and Reference Safety Information (RSI for assigned products, including regulatory responsibilities in associated change control and labeling processes.
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Knowledge of SEC/FINRA/CFTC/NFA and other US based regulatory rules. Assist with surveillance of various regulatory reporting obligations, including: CAT, TRACE, LOPR, Swap Dealer Trade Reporting.
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CCRP - Cert Clin Research Prof (Preferred) or RAC - Regulatory Affairs Cert (Preferred) 2 Years experience in a regulatory role or 4 Years experience in related clinical research role (Required.
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Experience analyzing compliance with regulatory programsrelated to water, wastewater and/or air quality. For more detailed information, refer to the Regulatory Compliance Specialist job description.
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This position will oversee all aspects of submission and continuous reporting to the relevant regulatory agencies, including the Institutional Review Board, the Food and Drug Administration, the Institutional Biosafety Committee, the institutional Radiation Safety Committee, and the pharmaceutical sponsor, funding foundation, or governmental agency.
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US Army Corps of Engineers (USACE) Office of the Chief of Engineers (OCE), responsible for the Army Nuclear Power Program, is ramping up to meet a wide range of operational, engineering, logistic regulatory certification and permitting requirements for future Operational Readiness Review (ORR) in accordance with Army Regulation 50-7 "Army Reactor Program" (ARP.
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Work closely with NGS production, Quality and PreClinical Genotox for compliant execution of genotoxicity data packages in support of regulatory filings and clinical programs. Interact with Health Authorities, in writing and verbally, including pre-submission (e.g., pre-IND), scientific advice filings, IND or CTA, meeting briefing books, or other requests from global regulatory authorities.
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We are looking for a regulatory specialist and permitting lead to support our clients in central and northern California. Work will include managing regulatory complexities and permitting for a range of projects, from municipal projects to large infrastructure programs, working with multidisciplinary teams of specialists, and performing both office and field work.
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Ensures all appropriate CMC regulatory aspects across teams to support change control requests including transfer of supply within GSK or with a 3rd party are delivered to agreed timelines. Scope of Responsibility·Will serve as a key strategic partner representing Global CMC Regulatory on Regulatory Networks and Matrix Teams, providing and overseeing strategic direction and guidance to Biopharmaceutical, Pharma Supply Chain, Clinical Trial Supply, Quality Assurance, and Commercial interfaces on both global project and key strategic business initiatives.
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Communicate updated requirements to the Compliance Integration team via the regulatory tracking tool in a clear and concise manner and coordinate with Mortgage Compliance Counsel on requests for further information or clarification.
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regulatory job Title: pharmacy technician Company: Rite Aid
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