Alessandra Luppi
About Alessandra Luppi
Alessandra Luppi is a Senior Clinical Trial Assistant and Regulatory Affairs Associate with extensive experience in clinical trial management. She has worked at Covance since 2016 and previously held various roles at Pfizer for 15 years.
Work at TFS HealthScience
Alessandra Luppi has been employed at TFS Trial Form Support since 2013. She holds the position of Senior Clinical Trial Assistant and Regulatory Affairs Associate. In this role, she contributes to the management and oversight of clinical trials, ensuring compliance with regulatory requirements. Her extensive experience in clinical trial administration supports her responsibilities in this position.
Work at Covance
Since 2016, Alessandra Luppi has worked at Covance as a Specialist 2 in Global Site Services. In this capacity, she is involved in supporting clinical trial operations on a global scale. Her role focuses on facilitating the processes necessary for the successful execution of clinical studies.
Experience at Pfizer
Alessandra Luppi spent 15 years at Pfizer, where she held multiple roles. From 1997 to 2012, she worked as a Clinical Trial Administrator. Additionally, she served as a Study Administrator Advisor for one year from 2011 to 2012. Her tenure also included a decade as a TMF Subject Matter Expert from 2002 to 2012, where she specialized in trial master file management.
Education and Expertise
Alessandra Luppi possesses significant expertise in clinical trial management and regulatory affairs. Her educational background supports her professional roles, equipping her with the necessary skills to navigate the complexities of clinical research and compliance. Her experience across various positions in the industry enhances her capabilities in supporting clinical trials.