Maura Naylor
About Maura Naylor
Maura Naylor: Director, Information & Data Management
Maura Naylor currently serves as the Director of Information & Data Management at Prevail. She has been with the company since 2016. In her role, she oversees the implementation of industry-standard technologies that support clinical research activities. Her responsibilities include managing technological strategies for a global EDC user base. Naylor's position requires her to ensure that the technologies employed meet stringent industry standards, ensuring efficient and effective data management in clinical trials.
Maura Naylor's Clinical Research Experience
Maura Naylor brings 8 years of clinical research experience to her role at Prevail. She has worked on global Phase I to Phase IV clinical trials across various therapeutic areas. This extensive experience has equipped her with a thorough understanding of the complexities and requirements involved in clinical research, from early-stage trials to late-stage studies. Her expertise contributes significantly to the successful management of clinical data and the implementation of advanced technologies at Prevail.
Maura Naylor's Education and Expertise
Maura Naylor holds a Bachelor of Science Degree in Biology from Temple University. She further advanced her academic credentials by obtaining a Master of Science Degree in Biomedical Sciences from Thomas Jefferson University. Her educational background provides a strong foundation for her work in clinical research and data management. The combination of theoretical knowledge and practical experience positions her well to lead initiatives that require both scientific understanding and technical acumen.
Maura Naylor at Prevail
Since joining Prevail in 2016, Maura Naylor has played a crucial role in advancing the company's clinical research capabilities. She is responsible for ensuring that all technological implementations align with industry standards, thereby supporting various clinical research activities. Her role involves managing a global user base for EDC systems, ensuring that data collection and management processes are robust and efficient. Her contributions help streamline clinical trials, improving both accuracy and compliance in data management.