Chris Mario
About Chris Mario
Chris Mario serves as the Director of Clinical Operations at Asklepios BioPharmaceutical, Inc., where he has worked since 2021. He has extensive experience in clinical operations, having held various roles at Voyager Therapeutics and Curis, and holds a Bachelor of Science in Psychology from Salem State University.
Current Role at Asklepios BioPharmaceutical
Chris Mario serves as the Director of Clinical Operations at Asklepios BioPharmaceutical, Inc. (AskBio) in the CNS Division. He has held this position since 2021, contributing to the management and oversight of clinical operations. His role involves ensuring compliance with regulatory requirements and maintaining high standards in clinical trial execution.
Previous Experience at Voyager Therapeutics
Chris Mario worked at Voyager Therapeutics, Inc. from 2015 to 2019, where he held multiple positions. He started as a Clinical Trial Associate for one year, then advanced to Clinical Trial Manager for two years, and subsequently served as Clinical Trial Manager II for seven months. His responsibilities included managing clinical trials and collaborating with various stakeholders to ensure successful trial outcomes.
Experience at Curis
From 2019 to 2021, Chris Mario worked as a Clinical Operations Consultant at Curis. In this role, he focused on enhancing clinical operations and supporting the development of clinical trial strategies. His expertise contributed to the effective management of clinical studies during this period.
Educational Background in Psychology
Chris Mario earned a Bachelor of Science degree in Psychology from Salem State University. His educational background provides a foundation for understanding patient behavior and enhancing recruitment strategies in clinical trials. Additionally, he has completed training at Barnett Seminars, furthering his knowledge in clinical operations.
Clinical Operations Skills and Expertise
Chris Mario has developed expertise in clinical operations, focusing on patient identification, recruitment, and enrollment strategies. He collaborates with clinical development teams and builds relationships with site investigators and coordinators. His skills include the development, review, and approval of critical study documents, ensuring compliance with Good Clinical Practice (GCP) guidelines.