tranScrip
Catherine Parker is an accomplished professional in regulatory affairs with extensive experience in the pharmaceutical industry. Currently serving as Senior Manager of Regulatory Affairs at tranScrip since April 2023, Parker has previously held the position of Senior Regulatory Affairs Consultant at Real Regulatory Ltd from September 2016 onward. Earlier roles include Regulatory Affairs Executive and Senior Regulatory Affairs Associate at Douglas Pharmaceuticals Ltd, as well as positions at Bayer HealthCare, Pacific Pharmaceuticals Ltd., Sanofi, and Quintiles. Parker holds a Master of Science in Pharmaceutical Analysis from Trinity College Dublin and a Bachelor of Science in Chemistry from University College Dublin.
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tranScrip
tranScrip is a leading contract drug development organisation which supports pharma and biotech companies in the development and lifecycle of medicines. We bring innovative solutions to clients’ global drug development needs. From translational medicine through to registration and post licencing, we deliver both strategic leadership and operational execution of development programmes, covering clinical, regulatory, drug safety, and commercial elements. Our teams of physicians, scientists and regulatory experts, help clients select the most promising drug candidates and bring them to the market. We guide our clients through their decision making from first in man studies to proof of concept and pivotal trials, regulatory submissions and product launches. In the last decade, tranScrip has supported over 250 clients and has been integral to many development programmes and regulatory submissions, bringing products to the market each year across a wide range of therapeutic areas.