Meet Nour Medjdoub, our new Clinical & Regulatory Affairs Specialist

We are excited to introduce Nour Medjdoub to our team, taking on the role of Clinical & Regulatory Affairs Specialist. Nour brings valuable experience and expertise from the healthcare and pharmaceutical sectors and has long been passionate about science.  

We asked her a few questions about her career path, what sparked her love for science, and what she will bring to her new role with us.

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1. What interests you most about science🎙️?

What draws me to science is its ability to truly improve lives and leave a lasting impact. I am passionate about how discoveries can lead to better health outcomes, sustainable solutions, and improved community well-being. It is inspiring to think that through scientific progress, we can contribute to the advancement of societies.

2. What is your background in (education/career trajectory) 🎙️?

I obtained my PharmD from the University of Oran 1 in Algeria, followed by a European Master’s in Translational Cosmetic and Dermatological Sciences (EMOTION MASTER) through an Erasmus Mundus program at the University of Eastern Piedmont “Amedeo Avogadro.” I then pursued a Master’s in Biomedical Sciences with a specialization in clinical research at the University of Namur. 

My experience includes working in a community pharmacy, where I focused on patient care and medication management. I learned how to assess patient needs, provide medication counseling, and educate patients about their treatments. This role helped me understand the importance of safe medication use and how to support patients in managing their health effectively. 

I have also gained experience in regulatory affairs and project management, by contributing to regulatory submissions, site qualification visits, and clinical trial documentation.

3. What excites you most about your role at IDEVAX 🎙️?

I am thrilled to join the IDEVAX team in the role of Clinical and Regulatory Affairs Specialist. It is a great opportunity to join a company at the forefront of developing innovative technologies to enhance vaccine efficacy and accessibility. I have been following IDEVAX for some time and have even explored internship opportunities  due to my admiration for their commitment to advancing immunization strategies.

In this role, I will be responsible for executing preclinical evaluations, planning and conducting clinical studies, and supporting post-market follow-up activities. I look forward to working with cross-functional teams to ensure compliance with regulatory standards and contributing to the development of new devices. Being part of a dedicated team committed to improving global health is truly inspiring, and I am eager to make a meaningful impact with IDEVAX.