Regulatory Affairs Specialist (Belgian Dutch) – Remote

Worldwide Clinical Trials; Belgique; À distance; EUR 42 000 - 62 000; Plein temps

Résumé du poste

Worldwide Clinical Trials is seeking a Regulatory Affairs Specialist to support submissions across Belgium, France, and the Netherlands. In this remote role, you will partner with cross-functional teams to ensure timely, compliant regulatory submissions and maintain alignment with local and international requirements.

The ideal candidate holds a bachelor’s degree in a life science and has at least one year of clinical research experience, with strong knowledge of ICH GCP and EU directives, plus

Qualifications

• Bachelor’s degree in a medical, biological, physical, health, pharmacy, or related science.
• 1+ year of clinical research experience, preferably in regulatory affairs or related function.
• Working knowledge of ICH GCP, EU Clinical Trials Directive, and regulatory guidance.

Responsabilités

• Coordinate regulatory submissions, ensuring documents are planned, compiled, tracked, and submitted on time.
• Communicate submission status, risks, and regulatory updates to study teams.

Connaissances

Regulatory submissions coordination

Regulatory expertise

Project management

Communication skills

Team collaboration

Formation

Bachelor's degree in a life science

Outils

Microsoft Office

Regulatory databases

Description du poste

Worldwide Clinical Trials is seeking a Regulatory Affairs Specialist to support submissions across Belgium, France, and the Netherlands. In this remote role, you will partner with cross-functional teams to ensure timely, compliant regulatory submissions and maintain alignment with local and international requirements.

The ideal candidate holds a bachelor’s degree in a life science and has at least one year of clinical research experience, with strong knowledge of ICH GCP and EU directives, plus