BeNeLux Regulatory Lead | RA, PV & Market Access

MAP Patient Access; Gent; Hybride; EUR 80 000 - 110 000; Plein temps

Avantages offerts par ce poste

Meal vouchers

13th month pay

Mobility budget

32 days leave

Résumé du poste

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.

Qualifications

• Master/PhD in science or equal through experience in pharma.
• Fluent English; Dutch/French/English language skills are essential.
• Experience in pharma company or regulatory/consulting environment.

Responsabilités

• Manage BeNeLux regulatory activities to obtain marketing authorizations.
• Support RIP (information and publicity) activities and local QPPV tasks.
• Contribute to reimbursement files and medical affairs projects.
• Coordinate medical information activities and stakeholder interactions.
• Engage with cross-border BeNeLux market access initiatives.

Connaissances

Regulatory affairs

Stakeholder management

Project management

Networking

Formation

Master's/PhD in science

Description du poste

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.