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
Can you bring your R&D expertise to our team? Join our team based in Hunedoara, Romania, and enjoy a collaborative culture that empowers you to build a career you can be proud of. What you would
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
About us : Helpware is a technology-driven American company with offices in the USA, Poland, Germany, Albania, Georgia, Ukraine, Mexico, Philippines, and Uganda, providing Customer Experience & Operational Support services for modern companies. Our team of
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 Manager
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
The Sr. Vendor Manager (SVM) is accountable for the evaluation, integration, oversight, and performance of all vendors that support Alimentiv’s clinical services, including a wide array of central lab vendors, central/local drug depots, and goods and