Melisa Moore
About Melisa Moore
Melisa Moore is a Senior Manager of Clinical Quality at Abeona Therapeutics, bringing over a decade of leadership experience in clinical compliance and quality management. She has held various roles in prominent companies, including Pharm-Olam, LLC and Thermo Fisher Scientific, and possesses a strong understanding of regulatory standards essential for clinical trials.
Current Role at Abeona Therapeutics
Melisa Moore serves as the Senior Manager of Clinical Quality at Abeona Therapeutics. She has held this position since 2021 and is responsible for overseeing clinical quality processes. Her role involves ensuring compliance with regulatory standards and maintaining the quality of clinical trials. Her leadership in this capacity contributes to the organization's commitment to delivering safe and effective therapies.
Previous Experience in Clinical Quality Management
Prior to her current role, Melisa Moore worked at Pharm-Olam, LLC, where she advanced from Manager of Compliance to Director of Compliance between 2017 and 2021. Her experience includes managing compliance initiatives and ensuring adherence to quality standards in clinical trials. Additionally, she held positions at Daiichi Sankyo, Inc. and Fisher Clinical Services, where she focused on quality assurance and regulatory coordination.
Educational Background
Melisa Moore has an educational background that includes an Associate's Degree in General Studies from Reading Area Community College, completed between 2015 and 2018. She furthered her education at Penn State College of Health and Human Development, obtaining a Bachelor of Science in Bio-Behavioral Health from 2018 to 2020. Her academic qualifications support her expertise in clinical quality and compliance.
Expertise in Clinical Compliance and Quality Standards
Melisa Moore possesses a decade of leadership experience in clinical compliance, quality, and risk management. She has a comprehensive understanding of cGLP, cGMP, GCP, and cGDP standards, which are essential for ensuring the quality and compliance of clinical trials. Her expertise also extends to cold chain distribution and storage, critical for maintaining the integrity of temperature-sensitive clinical products.
Career Progression and Relevant Roles
Throughout her career, Melisa Moore has held various roles that have contributed to her expertise in clinical quality management. She worked at Thermo Fisher Scientific as an Associate Quality Assurance Professional and Training Coordinator, and later as a Learning Management System Administrator. Her earlier role as an Environmental & Safety Compliance Specialist at Leading Edge Aviation Services further developed her compliance skills.