yeferson David Parra Ortiz

With nearly three years of experience as Clinical Research Associate (CRA), has contributed effectively to the planning, execution, and oversight of high-impact clinical studies. The role often involves coordination with interdisciplinary teams, ensuring compliance with regulations and ethical guidelines, managing progress reports, and overseeing the collection and analysis of critical clinical data. Excels under pressure and efficiently handles multiple tasks and projects simultaneously. Committed to continuous improvement, always staying up-to-date with the latest trends and regulations in clinical research, and striving to maintain the highest standards of data integrity and patient safety.

I am a biologist and clinical research professional with nearly three years of experience as a Clinical Research Associate (CRA). I have a solid track record in managing clinical studies, with a strong focus on coordinating interdisciplinary teams, ensuring regulatory compliance, and optimizing start-up processes in clinical trials.

Throughout my career, I have worked on studies related to vaccines (COVID-19 and MPOX), cardiology (CARED), and observational projects, ensuring their proper execution in alignment with local and international regulations (ICH-GCP). I have experience supervising regulatory documentation, reporting adverse events, and collaborating closely with research sites to ensure efficient operations and adherence to established timelines.

undergraduate in Biology

Diploma in monitoring of clinical studies and medical devices