The Senior Regulatory and Start Up Specialist will be responsible for managing regulatory submissions and site start-up activities for clinical trials in Argentina. This includes preparing Clinical Trial Application Forms, interacting with Competent Authorities and Ethics Committees, and ensuring compliance with local and international regulations. The role also involves mentoring junior staff, maintaining project plans, and collaborating with various teams to ensure timely site activation.
See how your résumé matches this role — and tailor it from what actually gets interviews.