The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executes multidivisi...
read moreSenior Associate, US Regulatory Affairs - Advertising & Promotion. The Senior Associate is responsible, when appropriate, for managing and coordinating regulatory activities associated with filing of ...
read moreThe Associate Director, Advertising and Promotion, Prescription Drug Products, reviews, approves and monitors prescription drug product advertising and promotional labeling pieces for compliance with ...
read moreSenior Associate, US Regulatory Affairs - Advertising & Promotion. The Senior Associate is responsible, when appropriate, for managing and coordinating regulatory activities associated with filing of ...
read moreImplements regulatory strategies and solutions to assure all advertising and promotional materials are in compliance with regulatory requirements and company policies. Works closely with the Regulator...
read moreImplements regulatory strategies and solutions to assure all advertising and promotional materials are in compliance with regulatory requirements and company policies. Works closely with the Regulator...
read moreJob Description Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across cros...
read moreThe Senior Associate is responsible, when appropriate, for managing and coordinating regulatory activities associated with filing of A&P materials to the USDA/CVB and FDA/CVM. Senior Associate, US Reg...
read moreWorking closely with senior management, the Regulatory Affairs Associate will:. Coordinate provider communications related to audits, surveys, compliance attestations, and other regulatory needs. Diss...
read moreThe Senior Associate is responsible, when appropriate, for managing and coordinating regulatory activities associated with filing of A&P materials to the USDA/CVB and FDA/CVM. Senior Associate, US Reg...
read moreWorking closely with senior management, the Regulatory Affairs Associate will:. Coordinate provider communications related to audits, surveys, compliance attestations, and other regulatory needs. Diss...
read moreThe Senior Associate is responsible, when appropriate, for managing and coordinating regulatory activities associated with filing of A&P materials to the USDA/CVB and FDA/CVM. Senior Associate, US Reg...
read moreThe Regulatory Affairs Associate will support the regulatory functions for a global medical device company. Provide regulatory guidance during the design and development phases of new medical devices,...
read moreSenior Associate, US Regulatory Affairs - Advertising & Promotion. The Senior Associate is responsible, when appropriate, for managing and coordinating regulatory activities associated with filing of ...
read moreThe Regulatory Affairs Associate will support the regulatory functions for a global medical device company. Maintain up-to-date product regulatory files, ensuring all documentation is current, accurat...
read moreThe Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivis...
read moreThe Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivis...
read moreThe Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivis...
read moreThe Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivis...
read moreThe Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivis...
read moreThe Regulatory Affairs Associate will support the regulatory functions for a global medical device company. Regulatory Submissions: Assist in preparing and submitting regulatory filings for medical de...
read moreImplements regulatory strategies and solutions to assure all advertising and promotional materials are in compliance with regulatory requirements and company policies. Works closely with the Regulator...
read moreResponsibilities:Provides strategic and operational leadership in advertising and promotion for the US market in accordance with business goals and objectives, FDA regulation, ICH guidelines, PhRMA gu...
read moreThe Regulatory Affairs Associate (Compliance Medical Auditor) supports. Maintain a current working knowledge on regulatory requirements associated with professional coding, billing, documentation, and...
read moreThe Regulatory Affairs Associate (Compliance Medical Auditor) supports. Maintain a current working knowledge on regulatory requirements associated with professional coding, billing, documentation, and...
read moreEnsure global development plans will meet global regulatory requirements by soliciting and integrating regional regulatory strategy liaison input. US Medical Device Regulatory Affairs experience. Resp...
read moreEnsure global development plans will meet global regulatory requirements by soliciting and integrating regional regulatory strategy liaison input. US Medical Device Regulatory Affairs experience. Resp...
read moreThis role is the key in ensuring the accurate and the timely submission of all Guerbet regulatory documents, staying current on all US federal regulations to ensure compliance, develop training progra...
read moreThis role is the key in ensuring the accurate and the timely submission of all Guerbet regulatory documents, staying current on all US federal regulations to ensure compliance, develop training progra...
read moreManager/Associate Director, Regulatory Strategist is responsible for the assigned branded programs and all strategic decisions to include providing regulatory pathway for the development, preview of c...
read moreSolid review, writing and communication skills and the ability to work independently in preparation of regulatory documents and correspondence. This role is responsible for the preparation of various ...
read moreThe Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prest...
read moreThe Regulatory Associate will report to the Senior Manager, Regulatory Affairs and, under the direction and guidance of the Associate Vice President, will help to ensure regulatory compliance of Prest...
read moreStrong business acumen and the ability to see business drivers outside of regulatory affairs. The Associate Director, Advertising and Promotion, Prescription Drug Products, reviews, approves and monit...
read moreStrong business acumen and the ability to see business drivers outside of regulatory affairs. The Associate Director, Advertising and Promotion, Prescription Drug Products, reviews, approves and monit...
read moreSignificant experience contributing to the development of commercial regulatory or related strategies, leading cross-functional regulatory activities, and representing Regulatory to cross-functional t...
read moreSignificant experience contributing to the development of commercial regulatory or related strategies, leading cross-functional regulatory activities, and representing Regulatory to cross-functional t...
read moreAssociate Director/Director, Regulatory Affairs. Must have at least 5 years in regulatory affairs leading strategy development and implementation in a cross-functional project team setting. Experience...
read moreThe Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely...
read moreThe Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely...
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