Melisa Clark
About Melisa Clark
Melisa Clark is a Senior Regulatory Affairs Manager at WEP Clinical, specializing in expanded access and FDA regulatory affairs for drugs, biologics, and medical devices. She has extensive experience in regulatory roles at the University of Arkansas for Medical Sciences and possesses skills in translation and cognitive ergonomics.
Work at WEP Clinical
Melisa Clark currently holds the position of Senior Regulatory Affairs Manager at WEP Clinical, a role she has occupied since 2023. Prior to this, she worked as a Senior Project Manager at the same organization from 2022 to 2023 for a duration of 10 months. Her work at WEP Clinical is conducted remotely from Little Rock, Arkansas, United States.
Education and Expertise
Melisa Clark earned her Bachelor of Arts in French with Honors from the University of Central Arkansas, studying from 1995 to 2000. She furthered her education at Université Lumière Lyon 2, where she obtained a Licence in Cognitive Science from 2004 to 2005 and a Masters2 in Applied Cognitive Science from 2005 to 2008. Her expertise includes expanded access and FDA regulatory affairs for drugs, biologics, and medical devices, as well as cognitive ergonomics for information and communication technology.
Background
Melisa Clark has a diverse professional background primarily centered around regulatory affairs and quality assurance in the healthcare sector. She worked at the University of Arkansas for Medical Sciences (UAMS) in various roles, including Interim Quality Assurance, Regulatory Affairs Manager, and Regulatory Specialist, from 2011 to 2022. Her experience also includes working as a Technical Translator at Kelly Scientific Resources in France and as an English Assistant at Education Nationale.
Achievements
Throughout her career, Melisa Clark has developed significant expertise in regulatory submissions, including IND/IDE submission and management. She has experience in project management and protocol development, particularly in the fields of hematology-oncology and clinical trials. Her skills also extend to data mining and data entry for medical databases, showcasing her comprehensive understanding of regulatory processes.