This role will be key to further develop the country capabilities in clinical research. Under the oversight of the country or cluster CRD the person will be responsible for the end to end performance of clinical trials in 1 or several TA, from feasibility to close out in 1 or several countries. The
Major Activities Major activities include, but are not limited to: New MA applications for assigned products: Performs timely and correct submission and approval of assigned new Marketing Authorization applications in close cooperation with relevant persons in the managing, medical, finance, custome
Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compl