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Reporting to the Associate Director of Regulatory Affairs, the Veeva Quality Assurance Lead will serve as a lead for the Veeva Quality Assurance Specialists in day to day operations, will review, itemize and migrate all regulatory documentation from the current document management system to the SiteVault platform.
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Support authoring and manage document workflows for planned major submissions including health authority meeting packages, original INDs/CTAs, and protocol amendments:· Lead interactions with external regulatory submissions vendor· Collaborate with internal project team to facilitate IND/CTA document authoring and review workflows including SharePoint and Master Control responsibilities for regulatory affairs and CMC regulatory.
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The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
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The Associate Vice President for Student Success & Advocacy & Dean of Students (AVP/DOS) is a pivotal leadership role within the Division of Student Affairs, responsible for overseeing various departments focused on enhancing the student experience and promoting a supportive campus environment.
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Piper Companies is currently seeking a Regulatory Affairs Specialist, Cell & Gene Therapy for an opportunity in Philadelphia, Pennsylvania (PA), to join an innovative biotechnology company creating life-saving cell therapies.
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Develops/Reviews Stormwater Management Reports and Stormwater Pollution Prevention Plans (SWPPP) to support regulatory permits; Conversant with regulatory codes, design codes and standards, best management practices, permit requirements and construction practices.
$93,400 - $155,100 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
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An appreciation of regulatory expectations for model risk management is desirable. Advises and prepares reports on risk, control, and governance related topicsProactively identifies, evaluates, and recommends improvements to strengthen model risk management and enhance risk identification and oversightMaintains understanding of industry trends in model validation and provide updates to stakeholder teams to enhance the knowledge and awareness or best practicesParticipates in special projects and performs other duties as assigned.
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The EHS Specialist I will also be responsible for support and enforcement of regulatory requirements for healthcare from the Joint Commission, the PA Department of Health, OSHA and local codes and ordinances.
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Performs and documents regular assessments of regulatory and code compliance, hazardous operations and the general condition/operation of the facility for development of safety concerns, issues or unsafe practices.
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Communicate frequently with other Respiratory Sales Specialists across the country and cross-functional counterparts such as Marketing, Sales Ops, Market Access, Field Reimbursement, Training, and Medical Affairs to create alignment of business plan, focus on strategic drivers, and sharing best practices.
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Must be a law school graduate with an LLB or JD degree Must be admitted to the Pennsylvania Bar.5 or more years of experience working with laws and regulations related to litigation, commercial, energy, and/or regulatory law.
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Job Description Position Summary: The Regulatory Law Unit’s Water Division is currently seeking a licensed Pennsylvania Attorney to fill an Assistant City Solicitor or Deputy City Solicitor position.
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Transamerica is organized by lines of business (Life Insurance, Annuities, Mutual Funds, Retirement Plans, and Employee Benefits), which are supported by Transamerica Corporate (Corporate Development; Finance; Internal Audit; Legislative, Regulatory & Policy; Office of the CEO; People and Places; Brand; Corporate Affairs; Risk; and Technology.
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Seeking an experienced Contract & Business Affairs Director to manage & negotiate complex multi-party contracts within the media/entertainment/content streaming industry. Disseminating relevant contract summaries and partner updates across key internal stakeholders including content operations, editorial, ad operations, finance, and legal Prepare business term sheets and contract analysis for upcoming deal negotiations and inquiries from senior management.
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regulatory affairs jobs Title: regulatory specialist in Philadelphia, PA
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