I work as a Clinical Data Programmer at a leading Contract Research Organization (CRO), contributing to the management and quality control of clinical data for pharmaceutical and biotech research studies. Over the past two years, I’ve supported global healthcare solutions by programming data manipulations, integrating external data sources, and preparing SAS datasets for regulatory submissions like the FDA.With a Master’s degree in Pharmaceutical Sciences, specializing in research and development, I’ve sharpened my skills in data science, machine learning, and data visualization. I hold certifications in Python, SAS, and Data Science, which I leverage to enhance data quality and improve clinical trial efficiency. My personal projects, shared on my website and GitHub, reflect my passion for innovation and the application of data science in healthcare.Additionally, my MSc in Drug Discovery and Development equipped me with a strong understanding of regulatory frameworks, clinical trial processes, and the importance of compliance in drug development. My focus now extends to the intersection of AI and legal compliance, particularly the EU AI Act. I aim to help organizations navigate AI regulations and ensure ethical and effective AI applications, especially in healthcare.Key Responsibilities: