Hanna is a Global Quality and Regulatory Compliance Expert and Innovation Strategist with over 20 years of versatile experience in clinical trials across global processes and functions in the Pharma and CRO industries. She has worked in multi-cultural environments in the EMEA, NA, and APAC regions.
Hanna is a skilled leader in Quality and Compliance Strategy, Quality Assurance, Inspection Readiness, Quality Management System, GCP/GxP Audit Programme, Quality Culture, Risk Management, Process and Operational Excellence, and Vendor Management. She also has extensive knowledge and experience in Agile Project Management, Clinical Operations, and Change Management as well as a Decentralised Clinical Trial, Digital Transformation, and Business Integration.
In addition to her leadership roles, Hanna is also a qualified lecturer and trainer. She supports various projects and initiatives led by the Research Quality Association, TransCelerate, Institute of Clinical Research, European Forum GCP, as well as led by Regulatory Authorities.
Hanna is the author and co-author of numerous articles related to clinical trials and the books ‘Clinical Trials – Challenges and Development Prospects’ and ‘Clinical Trials – practice, law, ethics.
