A Bit About Us: Are you an exemplary Director level US Regulatory Advertising and Promotion? This person will lead and manage regulatory strategies for advertising, promotion, and labeling activities of our products in the U.S. You will be responsible for ensuring all promotional materials and activities comply with applicable U.S. regulations, including FDA guidelines and other regulatory requirements. Day to day: • Lead the regulatory review as a member of the MLR review team of advertising and promotional materials for compliance with FDA, FTC, and other applicable U.S. regulations, guidelines, and internal company standards and policies. • Strong understanding of FDA regulations, particularly with respect to the advertising and promotion of prescription drugs, biologics, or medical devices. • Experience with the FDA’s promotional review process, including Form FDA 2253 submissions and labeling guidance.
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