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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.
$5,700 - $6,800 a monthFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Participates in the coordination and completion of multidisciplinary efforts in regard to regulatory preparedness and completion of applications (e.g. Hospital Accreditation and Licensure, CMS Database Forms, ICM completion, measurement of success data, DPH/DOH or CMS corrective action plans, and clinical charter teams.
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You will provide global product stewardship and regulatory affairs services for a line of chemical products that support Videojet printers. Manage our SDS, label, and regulatory affairs systems.
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Provide chemical regulatory support to:Ink development and maintenance of line teams. Demonstrated experience related to Production of SDS and Labels; Implementing compliance systems for global chemical regulations; Providing regulatory support to cross-functional teams.
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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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The Regulatory Engineer will support the Compliance Manager in problem resolution between safety agencies and company. Represent company’s interests by participation in Standards Development Committees, and inform appropriate internal organizations of latest regulatory requirements.
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Submitting permit applications via online portals for Client projects to regulatory agencies (DDOT, DOB, DOEE, etc. InterAgency is seeking a full time Regulatory Compliance Specialist to support a large civil infrastructure program in Washington DC, on permitting and regulatory compliance.
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Maintains awareness of regulatory legislation and assesses its impact on business and product development programs. The Manager/Associate Director, Health Economics and Outcomes Research (HEOR) Hepatology/Virology will join a high caliber team to execute HEOR strategies and tactics for Hepatitis C and early pipeline assets in virology.
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Provide regulatory guidance for Flight Operations, Inflight and Airport Customer Service related regulations such as 14 CFR Parts 21, 25, 43, 45,and 121. Review regulatory procedures as applicable to Flight Operations, Inflight and Airport Customer Service policies and procedures implemented by Frontier Airlines.
$84,280 - $105,350Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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BryceTech is looking for an experienced Regulatory Affairs Analyst to support the DHS FEMA, Office of Response and Recovery, CBRN program, supporting the Office of Emerging Threats Professional and Technical Services Contract.
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They will be responsible for coordinating submissions to local regulatory bodies including the Institutional Review Board (IRB) under the supervision of the Regulatory Affairs Manager. Responsibilities The Regulatory Affairs Associate ensures proper oversight of investigator-initiated clinical research and lab-based studies.
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Capability in managing deliverables essential for regulatory permit applications, CEQA documents, and environmental due diligence investigations (e.g., wetland delineations, rare plant surveys, habitat assessments, biological resources technical reports.
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Reporting to the Regulatory Affairs Manager, the Regulatory Affairs Specialist will, with minimal supervision, prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees- including new submissions, continuing reviews, amendments, adverse events, and reportable events.
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Reporting to the Regulatory Affairs Research Teams Manager, the Regulatory Affairs Specialist will, with minimal supervision , prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committees- including new submissions, continuing reviews, amendments, adverse events, and reportable events.
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Develop CMC regulatory strategy for early-stage cell therapy products through late stage and product registration. Lead the build out CMC regulatory organization to support expanding cell therapy pipeline.
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regulatory job Title: pharmacy technician Company: Cvs Health Retail
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