Site Activation Lead – Chile (Regulatory & Start-Up Expert)

Syneos - Clinical and Corporate - Prod is seeking a Site Activation Specialist II to manage the start-up of investigative sites across all phases of clinical trials in Chile. In this role, you will ensure timely and quality delivery of submissions to regulatory authorities and effectively monitor project compliance with agreed timelines and budgets.

The ideal candidate will contribute to continuous improvement efforts for site start-up components and act as a key contact with essential regulatory parties. You will be responsible for preparing essential documents and overseeing their submission as required by local regulations.