The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions
The Senior Clinical Analyst and Programmer will lead the programming activities for various purposes including different data listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Senior Clinical Analyst
Work from anywhere, impact everywhere : Diversity is at the heart of who we are at Xapo Bank. - Were a fully distributed team of over 160 Xapiens that work remotely from 50+ countries around the
More specifically, the Start-Up, Project Manager - Manage the end-to-end study start-up process, including site selection, regulatory submissions, site contracting and budgeting, and site activation. - Define start-up strategy and timelines in collaboration with the Project
As a Senior Clinical Data Manager, you will ensure that data captured in multiple clinical trials undertaken or managed by Indero is collected, managed, and reported clearly, accurately and securely. This role will be perfect for
Be part of something bigger! : As the world and the way people live is changing, we at Bekaert believe it’s our responsibility to contribute to finding new solutions for the future. With a 140+ year