MBChB, FFPM
Sarah is a pharmaceutical physician and drug safety expert with more than 30 years of industry experience. She has diverse pharmaceutical industry experience gained in big pharma, including Roche, Bristol-Myers Squibb and SmithKline Beecham.
Sarah qualified in medicine at the University of Ghana. Before joining the industry, she spent several years as an anaesthetist in the UK National Health Service.
Prior to joining tranScrip, she was the EU Qualified Person for Pharmacovigilance at Roche.
At tranScrip, Sarah heads up drug safety. As a seasoned clinical safety physician she has been the clinical safety lead for several successful indication expansion programs in the oncology arena, including breast cancer and Non-Hodgkin’s Lymphoma. She has also provided safety support in various clinical developmental programs including prostate cancer, malignant melanoma, community acquired pneumonia, and more recently COVID-19 trials.
She is a fellow of the Faculty of Pharmaceutical Medicine.
We are always interested to hear from experienced professionals that are looking to develop their career with tranScrip.
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