# Regulatory and Start Up Specialist - Netherlands

Hiring organization: [IQVIA](https://career.thegoodapps.co/organizations/iqvia)

Canonical page: https://career.thegoodapps.co/jobs/e8684fdd-b5cf-4b2e-bb6e-2b93e4567182

Listed on IQVIA's own careers site. Applications go to them directly.

- Seniority: Senior

## Summary

This role supports the clinical trial site activation process in the Netherlands, managing regulatory submissions, documentation, and stakeholder coordination to ensure trials launch efficiently and compliantly. It suits experienced clinical research professionals who are comfortable navigating European regulatory frameworks and acting as the liaison between trial sponsors, research sites, and internal teams.

_Our summary, not IQVIA's wording._

## Required

- Bachelor's degree in Life Sciences or related scientific discipline
- 3.5 to 5 years of clinical research experience
- Site activation expertise
- Regulatory submissions experience
- Contract negotiation experience
- Knowledge of Belgian and international clinical trial regulations
- Fluency in Dutch
- Strong English communication skills

Apply on IQVIA's site: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Amsterdam-Netherlands/Regulatory-and-Start-Up-Specialist---Netherlands_R1547012