Anuta Scridon

Background

About Anuta Scridon

Welcome! I’m Anuca - a curious and passionate person dedicated to understanding and improving the world around me. Daily, I combine detailed analysis with strategic action to ensure precision and quality in everything I do. I currently work as a (), overseeing and managing Phase clinical trials while ensuring compliance with regulations and best practices. I have experience in monitoring and site activation, collaborating cross-functionally with medical teams and investigators to ensure studies are conducted efficiently and ethically. My extensive knowledge of CRFs such as iMedidata, RAVE, inForm, and Zelta allows me to optimize processes and enhance clinical data management. ‍ I also have over 2 years of experience as a in Phase I oncology trials, which has provided me with a strong foundation in clinical data handling and validation, query resolution, and adverse event tracking. During this time, I also had the opportunity to work as a, ensuring site activation by overseeing 16 site initiation visits for various sponsors. Additionally, I also had the chance to share my expertise with the future of the industry by teaching a class on "Administrative Management of Clinical Trials" at ESAME Business School. During my Master’s in Clinical Trials, I researched the impact of Artificial Intelligence in Phase I clinical trials, and now I am expanding my skill set with a Master’s in. I enjoy working in dynamic environments where there is always something new to learn. My experience in clinical research, teaching, and volunteering has allowed me to adapt to different scenarios while always striving to add value and contribute to healthcare advancements. If we share interests or can collaborate on a project, I’d love to connect!