Medical Operations Lead

Nuwhï; Waver; Sur place; EUR 90 000 - 130 000; Plein temps

Résumé du poste

Nuwhï is seeking an experienced Medical Affairs professional in Belgium to own key medical operations and serve as the official RIP for the Belgian organisation. You will bridge medical affairs, compliance, and operations while ensuring material review, advertising approvals, and regulatory alignment.

The role requires a strong scientific background and official RIP certification from FAMHP. Fluency in Dutch, French and English is essential to collaborate across functions and with external

Qualifications

• Certified RIP by Belgium's FAMHP for medicinal products.
• Significant experience in medical affairs and regulatory compliance.
• Ability to manage timelines and influence stakeholders across functions.
• Fluent in Dutch, French and English as required.

Responsabilités

• Reviewing, approving and legally certifying promotional and non-promotional materials
• Ensuring compliance of materials and external activities with local legislation and applicable codes of practice
• Acting as RIP subject matter expert for RIP procedures and requirements
• Approving advertising projects
• Overseeing the training of representatives interacting with healthcare professionals
• Ensuring compliance with regulations related to pharmaceutical samples
• Leading Medical Information activities and supporting the team

Connaissances

Regulatory compliance

RIP certification

Medical affairs

Stakeholder management

Training oversight

Material review & approval

Dutch fluency

French fluency

English fluency

Description du poste

For one of our clients in the pharmaceutical industry, we are looking for an experienced Medical Affairs professional who combines strong scientific expertise with a solid understanding of the Belgian regulatory environment.

About the Role

This role sits at the intersection of Medical Affairs, compliance and operations. Reporting directly to the Country Medical Director, you will take ownership of key medical operations activities while acting as the officially certified Responsible for Information & Publicity (RIP) for the Belgian organisation.

Responsibilities

• Reviewing, approving and legally certifying promotional and non-promotional materials
• Ensuring compliance of materials and external activities with local legislation and applicable codes of practice
• Acting as the internal subject matter expert for RIP-related procedures and requirements
• Approving advertising projects
• Overseeing the training of representatives interacting with healthcare professionals
• Ensuring compliance with regulations related to pharmaceutical samples
• Leading Medical Information activities and supporting the team

Qualifications

You bring a strong scientific background and are officially certified by the Belgian Federal Agency for Medicines and Health Products (FAMHP) as Responsible for Pharmaceutical Information (RIP) for medicinal products for human use. Previous experience acting as RIP is a strong advantage.

Required Skills

You are comfortable working across functions and know how to combine regulatory rigour with a pragmatic, business-oriented approach. You can manage tight timelines, communicate clearly and influence stakeholders without necessarily having direct authority. Fluency in Dutch, French and English is required.