Sonia Guzzo

Offering strong foundation in analytical thinking and problem-solving. Knowledgeable about data collection, analysis, and interpretation with strong communication and organisational abilities. Ready to use and develop research, critical thinking, and collaborative skills in Clinical Research Associate role.

I'm writing to share my interest in the role of Clinical Research Associate (CRA) at this organization. With a Ph.D. in Translational Neuroscience and Neurotechnology and hands-on expertise in preclinical research, I am delighted about the opportunity to join your team and help create new therapeutics, thereby making a significant contribution to scientific progress. For someone like me who has battled Lupus for a long time and won many battles with the help of researchers, physicians, and clinical research assistance, the prospect of being an active participant in a process whose aim is the discovery of medications and treatments—that is, innovative care and hope—is what motivates me to want to become a CRA.

My academic experience has involved conducting extensive literature reviews and data analysis, which have helped me develop the critical thinking and analytical skills essential for a clinical research associate.  I possess strong organizational skills, attention to detail, and a proactive approach to problem solving. I am currently attending clinical research training, where I am gaining a fundamental understanding of clinical research principles, study design, and ethical considerations. Specifically, the topics I will be assimilating are as follows:

"Methodology and regulations of the clinical trial; Good Clinical Practice (GCP); the realities involved in the world of clinical research: pharmaceutical companies (sponsor), contract research organizations, the regulatory authorities, ethics committees, hospitals, and professionals involved in clinical trial management and monitoring; patient safety, data integrity, and protection of patient's data; the investigational medicinal product (IMP) and its management; tasks of the clinical monitor referred to in paragraph 5.18 of Annex 1 to the ministerial decree of July 15, 1997; different types of monitoring visits; experimental protocol and monitoring plan; Approach to Risk-Based Monitoring.”

I appreciate you taking the time to review my application. I am enthusiastic about the opportunity to join your team and contribute to significant clinical research. I look forward to discussing how my background, talents, and interests connect with your aims.

Microsoft Office Package, macOS, GraphPad Statistical Analysis

- MATLAB Fundamentals

- Practical and Theoretical course on animal care for scientific use

- AM and B Driving Licence