Regulatory Affairs Specialist, IQVIA Biotech

We are looking for a Regulatory Affairs professional to join our IQVIA Biotech Regulatory Affairs team, supporting clinical research projects across Europe. In this role, you will provide regulatory expertise and hands-on support throughout clinical development, with a particular focus on EU Clinical Trials Regulation (EU CTR) submissions. You will work as part of a global, project-based team supporting primarily drug development programs, including chemical entities and biologics. This is a gr…