Jingle T.
About Jingle T.
Jingle T. is an Associate Manager of Commercial Regulatory Affairs at BeiGene, with a background in regulatory writing and strategic marketing, and experience in project management.
Title at BeiGene
Jingle T. holds the position of Associate Manager, Commercial Regulatory Affairs at BeiGene. In this role, they have been working remotely since April 2022. Their responsibilities likely include overseeing regulatory compliance in commercial activities and ensuring that all promotional materials meet industry and legal standards.
Previous Role at Arthrex
From 2019 to 2022, Jingle T. worked as a Product Marketing Associate at Arthrex, where they were involved in product marketing strategies. Before that, they served as a Strategic Marketing Medical Writer for 6 months in 2019. Jingle also spent 6 years as a Medical Writer at Arthrex, based in Florida, from 2013 to 2019, focusing on medical and regulatory writing.
Early Career and Project Management Experience
Jingle T.'s early career includes a role as an Associate Project Manager at Synergy Medical Education, DDB Health, Omnicom Group Inc. from 2011 to 2013 in Pennsylvania. In this position, they gained significant project management experience, contributing to various healthcare education and marketing projects.
Educational Background
Jingle T. attained a Master of Business Administration (MBA) in Pharmaceutical and Healthcare Business from the University of the Sciences in Philadelphia, graduating in 2021. They also hold a Master of Science (MSc) in Biomedical Writing, focusing on regulatory writing for pharmaceuticals and medical devices. Additionally, they completed a Bachelor of Science (BSc) in subjects related to health science and sociology.
Experience in Regulatory Affairs and Remote Work
Jingle T. has extensive experience working in regulatory affairs, particularly in remotely managed roles. Their current position at BeiGene and previous roles have equipped them with expertise in regulatory writing and oversight of compliance processes. This skill set is crucial for ensuring that pharmaceutical and medical device companies adhere to industry standards.