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PURPOSE AND SCOPE:
Assists in...
Demonstrates 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 moreGenmab is looking for an Associate Director, Global Regulatory Affairs, Regulatory Strategy to be a part of our Global Regulatory Affairs organization. Evaluate regulatory risk and recommend mitigatio...
read moreSupports the regulatory function on development teams providing CMC regulatory guidance and strategy including identifying and assessing/mitigating regulatory risks. The Associate Director, Regulatory...
read moreSupports CMC regulatory affairs activities for marketed products and compounds in development in line with US and ex-US regulatory requirements. Supports the regulatory function on development teams p...
read moreSupports CMC regulatory affairs activities for marketed products and compounds in development in line with US and ex-US regulatory requirements. Supports the regulatory function on development teams p...
read moreSupports the regulatory function on development teams providing CMC regulatory guidance and strategy including identifying and assessing/mitigating regulatory risks. The Associate Director, Regulatory...
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 moreMore Years of direct regulatory affairs experience, including US labeling experience required. This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently pro...
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 moreThe Regulatory Affairs Associate will support the regulatory functions for a global medical device company. Assist in preparing and submitting regulatory filings for medical devices, including 510(k) ...
read moreThe Regulatory Affairs Associate will support the regulatory functions for a global medical device company. Assist in preparing and submitting regulatory filings for medical devices, including 510(k) ...
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 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 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 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 moreOur client is currently seeking a Associate Director, Regulatory Affairs Strategy. Serves as a regulatory lead to FDA and provides strategic input with the regional regulatory leads responsible for ex...
read moreServes as a regulatory lead to FDA and provides strategic input with the regional regulatory leads responsible for ex-US regulatory activities. Our client is currently seeking a Associate Director, Re...
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 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 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 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 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 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 moreAs our project portfolio at Genmab continues to grow, we are expanding our team and seeking a Team Lead, Associate Director to join the Regulatory Affairs CMC (RA CMC) team. We offer an exciting and c...
read moreThe Regulatory Affairs Associate (Compliance Medical Auditor) supports the functions of the Compliance Program for ENT and Allergy Associates, LLP, (ENTA) to be compliant with Federal and State guidel...
read moreThe Regulatory Affairs Associate (Compliance Medical Auditor) supports the functions of the Compliance Program for ENT and Allergy Associates, LLP, (ENTA) to be compliant with Federal and State guidel...
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 handles regulatory development and post-approval/regulatory compliance for assigned products. Develop a product regulatory timeline aligned to Bausch Health ...
read moreThe Associate Director, Regulatory Affairs handles regulatory development and post-approval/regulatory compliance for assigned products. Develop a product regulatory timeline aligned to Bausch Health ...
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 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 moreThis role is responsible for the preparation of various regulatory Labeling submissions and as well as review of labeling documents for submission. Electronically search for new regulatory guidelines ...
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 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 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 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...
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