MSc BSc
Regulatory Affairs
Sharon has seventeen years’ experience working within the pharmaceutical industry. Her early years was spent working in UK & IE site study start up and then moving specifically to the area of Regulatory Affairs.
Her areas of expertise lie in EU and ROW clinical trial regulatory management and requirements. She also has experience with EU labelling and EU lifecycle management of established products.
Sharon has a Masters degree in Immunology and Allergy and a Bachelors degree in Medical Sciences. She has worked as an inhouse consultant for a large innovator pharmaceutical company. In addition, Sharon has many years’ experience working in various large multinational CROs.
We invite you to explore exciting opportunities with us and become a part of a dynamic team dedicated to excellence. Share your expertise and embark on a rewarding journey with tranScrip.
Contact usOur experienced physicians and scientists, together with our regulatory, clinical and commercial experts can support you to maximise the value of your products. Whatever your project requires, we have the expertise to meet your needs.