Regulatory Affairs Officer, IQVIA Biotech

_At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patient impact. With dedicated teams, deep therapeutic expertise, and a biotech-tailored delivery model, we accelerate clinical development from early phase through global registrational studies._

**Job Overview**

As an experienced individual contributor within IQVIA Biotech’s Regulatory Affairs team, you’ll operate under limited supervision to drive clinical trial regulatory strategy and delivery across complex, multi‑stakeholder projects. You’ll lead cross‑functional regulatory workstreams, prepare and review clinical trial submission materials, and act as a clinical trial regulatory subject‑matter expert (SME) throughout the clinical trial lifecycle. You’ll build trusted relationships with sponsors, present at bid defenses, manage scope and budget for assigned projects, and contribute to team capability by reviewing SOPs and delivering targeted training. This role reports in...