Medical Operations Lead, RIP & Compliance

Nuwhï; Waver; Sur place; EUR 70 000 - 90 000; Plein temps

Résumé du poste

Nuwhï is seeking a qualified professional to own medical operations and serve as the officially certified Responsible for Information & Publicity (RIP) for Belgium. The role sits at the intersection of Medical Affairs, compliance and operations, reporting to the Country Medical Director.

You will review and certify promotional materials, ensure regulatory compliance, and lead Medical Information activities while training staff on material review requirements and systems such as Veeva.

Qualifications

• Strong scientific background; RIP certification by FAMHP for medicinal products for human use.
• Previous RIP experience is a strong advantage.
• Fluency in Dutch, French and English is required.

Responsabilités

• Review, approve and legally certify promotional and non-promotional materials.
• Ensure compliance of materials and external activities with local legislation and codes.
• Act as internal subject matter expert for RIP-related procedures and requirements.
• Approve advertising projects.
• Oversee training of representatives interacting with healthcare professionals.
• Ensure compliance with regulations related to pharmaceutical samples.
• Lead Medical Information activities and support the team.
• Coordinate planning and reporting processes across the Belgian organisation.

Connaissances

RIP certification

Scientific background

Regulatory compliance

Stakeholder influence

Veeva knowledge

Fluency in Dutch, French, English

Outils

Veeva system

Description du poste

Nuwhï is seeking a qualified professional to own medical operations and serve as the officially certified Responsible for Information & Publicity (RIP) for Belgium. The role sits at the intersection of Medical Affairs, compliance and operations, reporting to the Country Medical Director.

You will review and certify promotional materials, ensure regulatory compliance, and lead Medical Information activities while training staff on material review requirements and systems such as Veeva.