Job Description:As the Senior Manager Associate Director of Regulatory Affairs, Advertising and Promotion, you will report directly to the Senior Director, Regulatory Affairs. Associate Director of Re...
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 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 moreAssociate Director Regulatory Affairs, US Advertising and Promotion Job at AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today ...
read moreBS/BA in Life Sciences in a relevant field required; advanced degree strongly preferred (PharmD, MD, PhD) with 7-10 years of regulatory experience in the branded biotech/pharma industry supporting reg...
read moreEnsure global development plans will meet global regulatory requirements by soliciting and integrating regional regulatory strategy liaison input. Responsible for understanding the regulatory landscap...
read moreRegulatory Affairs Certified is a plus. Serves as a liaison to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. BS/BA in Life Sciences i...
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 moreKnowledge & Other RequirementsDemonstrates in-depth knowledge of current trends in regulatory affairs and is able to apply this to advance and accelerate regulatory strategies for assigned products or...
read moreJob DescriptionThe Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and execu...
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 moreMannKind Corporation has an opening for an Associate Director, CMC Regulatory Affairs in Danbury, CT. Associate Director, CMC Regulatory Affairs. At least 5 years of experience working with analysis a...
read moreMannKind Corporation has an opening for an Associate Director, CMC Regulatory Affairs in Danbury, CT. Associate Director, CMC Regulatory Affairs. At least 5 years of experience working with analysis a...
read moreThe Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide...
read moreThis position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Reg...
read moreWe are seeking an experienced and highly motivated Associate Director, Regulatory Affairs to support our expanding portfolio in the oncology area. Minimum of 5 years of regulatory affairs experience i...
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 moreServes as a regulatory lead to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. BS/BA in Life Sciences in a relevant field required; adv...
read moreServes as a regulatory lead to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. BS/BA in Life Sciences in a relevant field required; adv...
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 moreDemonstrates in-depth knowledge of current trends in regulatory affairs and is able to apply this to advance and accelerate regulatory strategies for assigned products or projects. Significant experie...
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 moreResponsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing strategies. Ensure global development plans will meet global regulatory requirements by ...
read moreResponsible for understanding the regulatory landscape, assessing regulatory risk, and developing global filing strategies. Ensure global development plans will meet global regulatory requirements by ...
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 Affairs Strategist. Manager/Associate Director, Regulatory Strategist is responsible for the assigned branded programs and all strategic decisions to include pro...
read moreManager/Associate Director, Regulatory Affairs Strategist. Manager/Associate Director, Regulatory Strategist is responsible for the assigned branded programs and all strategic decisions to include pro...
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 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 moreWorks closely with the Regulatory Affairs labeling group regarding package insert changes to assess and determine the impact of proposed labeling changes on product promotion. Broad knowledge of the p...
read moreDemonstrates in-depth knowledge of current trends in regulatory affairs and is able to apply this to advance and accelerate regulatory strategies for assigned products or projects. Significant experie...
read moreRegulatory 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 cross-functional teams. Sig...
read moreThe Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Utilize regulatory expertise and knowledge of regulatory requirements and r...
read moreRegulatory 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 cross-functional teams. Dem...
read moreAssociate Director/Director, Regulatory Affairs. Develops and maintains practices and procedures of Global Regulatory Affairs team. Must have at least 5 years in regulatory affairs leading strategy de...
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. Integrates...
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 more