In today’s blog, it is our pleasure to introduce you to Pauline Jacquety, Regulatory Affairs Senior Manager.
Hi Pauline, Can you tell us what is your role at SparingVision?
I am a Regulatory Affairs Senior Manager. My role focuses on coordinating the preparation, submission, and maintenance of regulatory dossiers for SparingVision’s interventional and non-interventional clinical studies.
What inspired you to join the genomic medicine in ophthalmic industry, and what keeps you motivated?
I was eager to explore and learn more about advanced therapies and genomic medicines, which I find scientifically fascinating and highly promising in areas where there are significant unmet medical needs.
What do you do in your department at SparingVision?
Our team is responsible for the development and implementation of global regulatory strategies for SparingVision’s gene therapy pipeline.
How do you work with different teams across the company?
I work in close collaboration with various teams, such as clinical, non-clinical, and CMC, which is essential to regulatory activities as each team’s input is critical to building high-quality regulatory dossiers.
We always say everything at SparingVision starts with the patient. What does that mean in your role?
Our mission in Regulatory Affairs is to enable patients to access innovative investigational therapies as quickly and safely as possible by securing and maintaining regulatory approvals across countries for our products in the clinical stages of development.
In a few words, why did you choose to work for SparingVision?
I find it very exciting to be part of a small, dynamic team that is constantly seeking solutions, working in a highly innovative environment, and dedicated to bringing hope to patients.
