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Advanced knowledge and understanding in the core areas of government affairs and policy (Stakeholder and Alliance Development, Government Relations, Political/Campaign experience, Access and Reimbursement Public Policy and Economic Analysis) to maximize colleague contributions.
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As an integral core member of cross functional teams the Senior Scientific Director provides strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.
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This new position will work closely with Global and Regional Market Access, HEOR, Marketing, Medical & Clinical Affairs, Research & Development, and Government Affairs colleagues to help ensure patients gain appropriate access to Abbott’s life changing point of care, rapid diagnostics.
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At Thermo Fisher Scientific, the Regulatory Affairs function plays a vital role in ensuring compliance with the ever-evolving global regulations governing our industries. Join our dynamic Regulatory Affairs team and contribute to our mission to enable our customers to make the world healthier, cleaner and safer.
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Obtain Licenses: Become a FINRA (Financial Industry Regulatory Authority) Registered Representative by studying for and obtaining your SIE, Series 7 Top Off and Series 66 licenses, fully paid for and sponsored by Fidelity.
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6+ years of progressive medical/scientific affairs experience within the pharmaceutical, biotech industry or at a consulting firm that supports the pharmaceutical or biotech industry; at least 3 years driving medical strategy.
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QMS, CAPA, change management, design control, Medical device, Iso 13485, product development, EU / MDSAP Regulations, Combination Products, regulatory affairs, Audits, Remediation. Regulatory affairs knowledge.
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6+ years of experience in Financial Services, Marketing, Compliance, Internal Audit Operations, Vendor Management areas, Operational and Regulatory or related field. Works as a liaison between Payments Risk and partners such as Operational Risk Management, Internal Audit, Third Party Risk Management, etc.
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5+ years of experience in external affairs, public affairs, government relations, political consulting, or related experience. Lead development and implementation of a public affairs strategy including community relations, stakeholder engagement and grassroots constituent support for the Company.
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Develop, maintain, document, and lead continuous improvement in regulatory programs including but not limited to items such as Arc Flash, LOTO, Confined Space and Process Safety Management (PSM.
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Experience working within Medical Affairs (MSL teams, CNE teams, Publications, Call Centers, etc.) Serves as a Medical Affairs reviewer in the CMLR (Commercial, Medical, Legal, Review) Committee.
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Closely work with Sales, Marketing, Procurement, & Regulatory to support category growth, supply continuity and vendor compliance. Conduct detailed analysis on the impact of pricing and assortment changes and execute findings and recommendations with the approval of Marketing & Merchandising Director.
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Accountable for leading a cross-functional asset team(s) including a medical, regulatory, CMC, research, operations, commercial, finance and data science to advance one or more assets from preclinical candidate nomination through clinical development, global/local regulatory submissions, and approval.
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Job Description Job Description · The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. · 4 years’ experience in Regulatory Affairs role.
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Floor & Decor strives to be the one-stop destination for our professional clients (PRO customer) in the hard surface flooring contractor space.
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regulatory affairs jobs Title: affairs specialist Company: Jazz Pharma in Deerfield, IL
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