Senior Director/AVP Regulatory Affairs CMC. As the AVP Regulatory CMC you will lead the Regulatory CMC team. Act as Rockets CMC representative to regulatory bodies, staying informed on industry trends...
read moreSenior Director/AVP Regulatory Affairs CMC. At least 10 years of regulatory affairs experience, specifically in CMC, with proven experience in managing CMC submissions. As the AVP Regulatory CMC you w...
read moreYou will report to the Senior Director of Regulatory Affairs CMC and be part of a team consisting of 8 experienced and dedicated colleagues. The project portfolio at Genmab is evolving, and we are loo...
read moreThe individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that...
read moreMore Years in regulatory affairs; experience in US regulatory affairs from IND through NDA/BLA required. Brings issues with regard to ways or working or resources to the Head of US Regulatory Affairs ...
read moreThe individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that...
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 moreThe Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives fo...
read moreThe Regulatory Affairs-Labeling, Associate Director is responsible for ensuring that Takeda gains regulatory approval for new products and product amendments, while maintaining the currency of product...
read moreIn this role, you will define the regulatory strategy for all products currently in the portfolio at various phases, to ensure the correct implementation of the regulatory strategy, to evaluate the re...
read moreIn this role, you will define the regulatory strategy for all products currently in the portfolio at various phases, to ensure the correct implementation of the regulatory strategy, to evaluate the re...
read moreResponsible for all regulatory affairs activities required to support lead, manage, review, and. Lead and manage all regulatory affairs-related activities for products. Maintain all regulatory files i...
read moreResponsible for all regulatory affairs activities required to support lead, manage, review, and. Lead and manage all regulatory affairs-related activities for products. Maintain all regulatory files i...
read moreExperience in regulatory affairs, focusing on medical device development. Hobson Prior is seeking a motivated Senior Regulatory Affairs Specialist focused on device development. Experience in preparin...
read moreThe Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Utilize regulatory expertise and knowledge of regulatory requirements and regulations...
read moreRA certification (by Regulatory Affairs Professional Society) is a plus. Leading the Regulatory Affairs and Compliance functions, this role will generate the preparation of submissions to obtain and m...
read moreThis role will be within Global Regulatory Affairs (GRA) and will report to the Sr Director, Labeling, Policy and Intelligence. The Global Regulatory Labeling Strategy Sr Manager/Associate Director wi...
read moreMedical Directors (Director/SD/ED levels) in Translational Medicine / Clinical Development / Medical Affairs / Drug Safety: 75+ retained assignments. Regulatory Affairs experience, with an emphasis in...
read moreMedical Directors (Director/SD/ED levels) in Translational Medicine / Clinical Development / Medical Affairs / Drug Safety: 75+ retained assignments. This hybrid role will lead US and Global regulator...
read moreMedical Directors (Director/SD/ED levels) in Translational Medicine / Clinical Development / Medical Affairs / Drug Safety: 75+ retained assignments. This hybrid role will lead US and Global regulator...
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