Listed on IQVIA’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
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. The full posting is on their site.
What they ask for
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