Senior Regulatory Affairs Coordinator
CurrentI work exclusively with the Thoracic Oncology department. In this role, I complete and submit study applications for the group and work on amendments and continuing reviews. I was the first person in this group to maintain studies after their initial IRB approval and currently, I manage over 15 studies. I maintain all regulatory, site, and investigator documents for the studies I manage, and I also manage the Veeva Vault electronic study binders for each study. In this role, I've begun training new staff in pre and post-study activation activities.