Maura Naylor

Maura Naylor's Title

Maura Naylor serves as the Director of Information & Data Management at Prevail. In this role, she oversees the implementation of cutting-edge technologies that conform to industry standards to support the clinical research activities of a global electronic data capture (EDC) user base. Her leadership ensures that the technological infrastructure is robust and efficient, facilitating the seamless execution of clinical trials.

Maura Naylor's Company

Since joining Prevail in 2016, Maura Naylor has significantly contributed to the company's mission. Prevail is a leading organization in the field of clinical research, dedicated to advancing medical science by conducting comprehensive clinical trials. Under Maura's guidance, Prevail has enhanced its technological capacity, supporting global Phase I to Phase IV clinical trials across various therapeutic areas.

Maura Naylor's Education and Expertise

Maura Naylor holds a Bachelor of Science in Biology from Temple University and a Master of Science in Biomedical Sciences from Thomas Jefferson University. This solid educational foundation has equipped her with the essential knowledge and skills to excel in the field of clinical research. Her expertise is evident in her ability to oversee complex data management systems and ensure compliance with industry standards.

Maura Naylor's Background

With 8 years of clinical research experience, Maura Naylor brings a wealth of knowledge to her role at Prevail. Her background includes working on global Phase I to Phase IV clinical trials in several therapeutic areas, providing her with a deep understanding of the clinical trial process from inception to completion. This experience has positioned her as a key player in the realm of data management and clinical research.

Maura Naylor's Achievements

Throughout her career, Maura Naylor has achieved significant milestones. Her leadership in implementing advanced technologies for clinical research has streamlined operations at Prevail, ensuring that global clinical trials are conducted efficiently and effectively. Her work has not only supported the success of numerous clinical trials but has also contributed to the broader field of medical research by enhancing data integrity and compliance.