Meghan Hanlon
About Meghan Hanlon
Meghan Hanlon serves as the Associate Director of Regulatory Affairs Advertising and Promotion at Mirati Therapeutics, bringing over 10 years of experience in the healthcare industry, particularly in the medical device and pharmaceutical sectors.
Current Role at Mirati Therapeutics
Meghan Hanlon serves as the Associate Director of Regulatory Affairs Advertising and Promotion at Mirati Therapeutics. She has held this position since 2022, contributing to the company's regulatory compliance efforts in advertising and promotional activities. Her role involves overseeing promotional materials and ensuring adherence to industry regulations, which is critical in the pharmaceutical sector.
Previous Experience at Pfizer
Prior to her current role, Meghan worked at Pfizer as the Compliance and Oversight Lead Manager from 2020 to 2022. In this position, she focused on compliance within the company's promotional practices, ensuring that all advertising efforts met regulatory standards. Her experience at Pfizer added to her extensive background in regulatory affairs.
Professional Background in Regulatory Affairs
Meghan has over 10 years of experience in the healthcare industry, specifically within the medical device and pharmaceutical sectors. She has held various roles that emphasize regulatory compliance, including her time as Regulatory Advertising & Promotional Manager at Array BioPharma Inc. from 2018 to 2020 and as Commercial Regulatory Process Manager at Medivation from 2015 to 2017.
Educational Qualifications
Meghan's educational background includes a Master’s degree in Integrated Marketing Communications from Golden Gate University, which she completed from 2009 to 2012. She also holds a Bachelor’s degree in Communication from Bryant University, earned between 2002 and 2006. Additionally, she studied Event and Meeting Planning at San Jose State University, achieving a certificate in 2006.
Skills and Expertise in Marketing and Compliance
Meghan possesses a strong background in branding development and product marketing collateral. She has engaged in Promotional and Medical Review Committees, contributing to global marketing communications. Her expertise includes streamlining user experience, managing digital asset processes, and ensuring compliance with OPDP submissions, which are essential for maintaining regulatory standards in advertising.