Dedicated and detail-oriented professional with a strong academic background and a passion for contributing to the advancement of healthcare through clinical trials. As a beginner in the field, I bring a solid foundation, coupled with a proactive approach to learning and adapting to the dynamic landscape of clinical research. Possessing a keen interest in ethical research practices and patient-centric outcomes, I am eager to leverage my theoretical knowledge and enthusiasm to make meaningful contributions to clinical trials. My academic coursework has equipped me with a comprehensive understanding of research methodologies, regulatory requirements, and the importance of maintaining data integrity throughout the trial process.
Good Clinical Practice (GCP) guidelines
Critical thinking analysis and decision making
Data collection and Report analysis
Detailed Documentation abilities