Pro-active mind-set and innovative thinker, to complement 5+ years of strong clinical expertise, from clinical trials to drug development. Ashleen acquires a strategic work ethic and high standard of adaptability, allowing her to tackle any regulatory issue faced. Having extensive experience in the clinical field, she has built meticulous regulatory knowledge to accompany her skills, allowing her to provide each regulatory solution efficiently and effectively.

Through completing her Bachelors and Masters in a scientific discipline, Ashleen has gained extensive clinical expertise and practical experience, for example when conducting clinical research on a range of human conditions. In doing so, she gained a strong familiarity with scientific concepts and clinical terminology, which she was able to apply to each of her work experience. For example, when completing her internship within clinical trials, she gained a broad range of knowledge, from regulatory standards to patient safety, which she can apply here at Eliquent to solve each regulatory issue faced.