Regulatory and Start Up Specialist - Belgium
IQVIA · Zaventem, Belgium +2 more
RegulatoryFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a regulatory specialist to manage site activation and country-level regulatory activities for clinical studies in Belgium. The role involves serving as primary contact for investigative sites, ensuring regulatory compliance, and coordinating documentation across project teams.
What they're looking for
- Fluency in Dutch and/or French language
- Experience with local regulatory submissions and contract negotiations
- Knowledge of site activation procedures and applicable regulations
- Familiarity with standard operating procedures and quality control processes
- Experience with clinical trial regulatory documentation and timelines
What you'll be doing
- Serve as single point of contact for assigned studies between sites, management, and project teams
- Prepare, review, and distribute site regulatory documents ensuring completeness and accuracy
- Perform site activation activities in compliance with regulations, SOPs, and work instructions
- Track and follow up on regulatory, ethics, ICF, and investigator pack document approvals
- Monitor site performance metrics and implement contingency plans as needed
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.