MSc BSc
Regulatory Affairs
Tessa has over thirteen years’ experience working within the pharmaceutical industry. She joined the company in July 2016 and has worked in regulatory affairs since then.
Her areas of expertise lie in clinical trial regulatory requirements, quality assurance, process-related validation, and analytical techniques. Tessa is also an experienced science writer and communicator.
Tessa has a masters degree in Science Communication and Public Engagement and a bachelors degree in Biology and Chemistry.
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.