Karen O'Hanlon PhD

Karen O’Hanlon is an experienced clinical project manager with over 12 years’ industry experience. She has managed clinical studies at Phase I & II, working with small molecule and biological development candidates. She is adept at medical writing, generating study documents including protocols, PIS, ICF and study reports, as well as regulatory submission documents, such as IBs and IMPDs. Karen provides hands-on support for CDDI’s Evidence-based Feasibility.

Previous roles include CPM at Medigene, Feasibility & Programme Manager and CPM at SRA Global Clinical Development, and Project Director at Retroscreen Virology. Karen holds a BSc in Medical Biochemistry and a PhD in Biochemistry.