Alicja Gietka

Alicja Gietka has extensive work experience in the clinical research industry. Alicja began their career as a Clinical Trial Assistant at Pfizer in 2011 and then moved on to AstraZeneca, where they held the positions of Global Study Associate and Global Study Associate Manager from 2012 to 2019. Alicja then joined DOCS as a Specialist in Central Monitoring, working on behalf of Janssen R&D. In 2020, Gietka joined Worldwide Clinical Trials as a Risk Manager, overseeing Risk-Based Quality Management. Currently, they serve as the Director of QbD Implementation at Accelsiors CRO.

Alicja Gietka holds a Master's Degree in Human Nutrition and Consumer Sciences, which they obtained from Szkoła Główna Gospodarstwa Wiejskiego w Warszawie from 2008 to 2009. Prior to that, they completed an Engineer's Degree in the Interdisciplinary Study of Environmental Conservation from the same institution from 2004 to 2008. Alicja also pursued a Postgraduate degree in Dietetics - the progress in human nutrition at the Food and Nutrition Institute from 2010 to 2011. In addition to their formal education, Alicja has obtained several certifications, including MyRBQM Essentials - Green Belt and MyRBQM® Academy | Risk-Based Quality Management Essentials - White Belt from Cyntegrity | Data Science for Clinical Trials in 2023 and 2022 respectively. Alicja also holds certification in Applied Project Management from Wenell Management, which they obtained in 2016.