eCommerce Strategy Director implements the policies and plans to execute the overall vision, strategy, and capacity needed to support organizational long-term and short-term e-commerce sales growth goals. Provides support for evaluating e-commerce investments & initiatives and facilitates the development of business cases and marketing plans. Being an eCommerce Strategy Director compiles data and analytics to study traffic, trends, customer touchpoints, and pain points used to analyze opportunities for innovation and expansion of customer engagement and revenue. Partners with stakeholders across the organization to optimize digital channels. Additionally, eCommerce Strategy Director plans and implements technical projects for improvements to customer experience, new e-commerce features and offerings. Requires a bachelor's degree. Typically reports to a director. The eCommerce Strategy Director typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be an eCommerce Strategy Director typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)
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Job DescriptionTakeda Development Center Americas, Inc. is seeking an Associate Director, Global Regulatory Affairs Strategy Lead in Cambridge, MA with the following requirements: Bachelor’s degree in Biology, Chemistry, Pharmacy or related field or foreign academic equivalent. 8 years of related experience. Prior experience must include: Lead the Global Regulatory Team (GRT) and applicable sub-working groups and serve as direct point of contact with the FDA, accountable for US FDA submissions, addressing agency queries leading to approvals, and lead agency meetings including meeting preparation (4 yrs); lead REMS activities and submissions especially on REMS KAB surveys and Assessment Report submitted to the US FDA (3 yrs); perform regulatory submissions in eCTD format, per ICH and FDA guidelines, and global regulatory requirements/submissions; lead local product labeling and Core data sheet process while providing strategic regulatory guidance as an SME (4 yrs). Up to 30% travel required.
Apply on-line at and search for Req # R0092069.
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LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull timeClear All
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