Summary : Provides contracting life cycle management and business solutions optimizing operational expertise to US MA US Medical Affairs, partnering with all areas in the end-to-end planning process and execution. Responsible for managing cross-functional teams in
The Study Start Up. Assocate II, collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles