About the Company
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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
Alongside your RIP responsibilities, you will help strengthen Medical Affairs operations and excellence across the Belgian organisation. You will coordinate key planning and reporting processes, support the implementation of Medical Infield Excellence, maintain Medical Affairs SOPs and train internal teams on material review requirements and systems such as Veeva.
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.
Interested?
If you have a Medical Affairs background and the required RIP certification, we would be happy to tell you more about the organisation, team and scope of the position. xqknzec
Feel free to reach out directly or send a message to @roxane Leloup for a confidential conversation.
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