This 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 moreShape new regulatory pathways in order to benefit stakeholders. Proven track record in regulatory leadership, including 505(b)(1), 505(b)(2), 505(j), etc. Strong regulatory knowledge of drug developme...
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 moreRegulatory Affairs Associate Director. Experience: 8 to 10 years regulatory affairs experience in the medical device industry. Partner with and actively support team, providing structure to ensure tha...
read moreThe Director of US Regulatory Affairs must be able to assess the project from a regulatory standpoint using a broad understanding of the FDA requirements and be able to prepare and maintain US submiss...
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 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 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 moreThe Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, and executing multidivisional initiatives fo...
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 moreMaintain all regulatory files information in compliance with regulatory authority. Lead and manage all regulatory affairs-related activities for products. Responsible for all regulatory affairs activi...
read moreThe Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulator...
read moreHobson Prior is seeking a motivated Senior Regulatory Affairs Specialist focused on device development. Experience in regulatory affairs, focusing on medical device development. This role requires a s...
read moreHobson Prior is seeking a motivated Senior Regulatory Affairs Specialist focused on device development. Experience in regulatory affairs, focusing on medical device development. This role requires a s...
read moreThe Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulator...
read moreLeading the Regulatory Affairs and Compliance functions, this role will generate the preparation of submissions to obtain and maintain approvals for commercially distributing products within the US. R...
read moreLeading the Regulatory Affairs and Compliance functions, this role will generate the preparation of submissions to obtain and maintain approvals for commercially distributing products within the US. R...
read moreAssess scientific information, regulatory precedent, competitive intelligence, and regulatory guidelines in order to make recommendations. DIRECTOR, GLOBAL REG AFFAIRS STRATEGY LEAD - ONCOLOGY. This h...
read moreMedical Directors (Director/SD/ED levels) in Translational Medicine / Clinical Development / Medical Affairs / Drug Safety: 75+ retained assignments. In depth working experience of US regulatory affai...
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