) VEEVA RIM Expert User GRA: o Coordinate all user activities regarding the tracking of regulatory events in relation with clinical trials & all global and local disclosure activities Act as GRA window
) VEEVA RIM Expert User GRA: o Coordinate all user activities regarding the tracking of regulatory events in relation with clinical trials & all global and local disclosure activities Act as GRA window
pricing.Quantify demand and growth for the product.Collaborate with Marketing and Subject Matter Experts to evolve/create new value & access offerings, including AI-driven solutions.Build and maintain external
role encompasses acting as a subject matter expert and thought leader for Regulatory Affairs in Europe (western and eastern). It covers regulatory affairs for all phases from drug development: pre-clin