BeNeLux Regulatory Lead | RA, PV & Market Access

MAP Patient Access in Ghent, Belgium, is seeking an experienced Regulatory Affairs professional to lead BeNeLux regulatory activities and contribute to medical affairs and market access projects. The role combines pharmacovigilance input, RIP activities, and stakeholder engagement in a dynamic European setting.

The position requires a Master/PhD in science or equivalent pharma experience, with fluency in Dutch, French and English. The role is hybrid, with one in-office day per week in Ghent.