Katarzyna Kozłowska
Katarzyna serves as a Clinical Research Associate II at Pure Clinical. She is responsible for monitoring clinical studies in accordance with ICH-GCP guidelines, ISO 20916:2019, Standard Operating Procedures, and all applicable regulations. She acts as a liaison between sponsors and clinical sites, providing support throughout the entire study process. Her duties include conducting monitoring visits and study-related training, verifying data quality, and ensuring procedural compliance with study protocols. She holds a degree in Laboratory Medicine from the Medical University of Łódź and a degree in Clinical and Biomedical Research from the Medical University of Poznań. She has two years of experience in clinical research.
Katarzyna Kozłowska
Education (2)
Medical University in Poznań
Postgraduate, Clinical and Biomedical Research
2021 – 2022
Medical University of Lodz
Master of Science (MSc), Department of Laboratory Medicine Master of Science (MSc), Department of Laboratory Medicine
2014 – 2019
Work Experience (4)
Pure Clinical
Clinical Research Associate II
VII 2024 – currently
Clinical Research Associate
I 2023 – VII 2024
Junior Clinical Specialist
IV 2022 – I 2023
Zakład Opiekuńczo-Leczniczy Szpital Uniwersytecki nr 1 im. dr. A. Jurasza
Clinical Trial Coordinator
X 2021 – IV 2022
GSK
Quality Assurance Specialist
I 2021 - X 2021
Courses (4)
Comarch
Project Management - Project Risk Management
Issued IX 2024
Microsoft Word - Optimization and Automation of Work with Documents. Advanced Course
Issued XI 2022
Brillance Sp. z o.o.
Monitoring of Clinical Trials - Course for CRAs and candidates for CRAs
Issued IX 2023
IQVIAIQVIA
ICH GCP Training for Investigators and Site Staff including ICH GCP E6 (R2)
Issued IV 2022