Manager, Regulatory Affairs
Dr Kim Champion is Regulatory Affairs Manager at Boyds.
With extensive experience in the Clinical Operations sphere, Kim’s role at Boyds includes preparing regulatory documentation and providing operational support to sponsors in all stages of drug development.
Kim’s career began in Switzerland, where she worked in hospital and private laboratories. After moving to England in 1990, she worked in Cambridge University laboratories (clinical and research) on the Addenbrooke’s campus before moving into Clinical Operations and working exclusively in Phase 1 & 2 clinical trials with advanced therapy medicinal products (ATMPs).
Kim worked for the European Society for Blood and Marrow Transplantation (EBMT) for 10 years, progressing from Trial Coordinator to Acting Director for Clinical Trials Operations. During this time, she built up the organisation’s clinical trials team and oversaw a portfolio of European phase 2-3 trials in cancer, haematological, neurological and autoimmune disorders, and had the opportunity to collaborate on projects with large companies, including Roche and Amgen as well as CROs.
In 2010, Kim joined University College London (UCL) as Regulatory Manager for ATMP trials in the Joint Research Office, where she supported scientists and physicians in bringing their academically developed ATMPs into the clinic. From there, she moved to the Cancer Research UK & UCL Cancer Trials Centre as a Trial Group Lead for ATMP trials, establishing UCL’s first trials team specialising solely in gene and cell therapies. While at UCL, she collaborated with companies such as Autolus and bluebird bio.
Kim has experience in developing all trail documents and has made CTA submissions in numerous Eruopean countries. She has a PhD in Molecular Haematology and was a Board member of the European Forum for Good Clinical Practice (EFGCP) as well as a member of a Research Ethics Committee at Kinds College London.
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