Charlene Tedde

Charlene TEDDE has a diverse work experience in the pharmaceutical industry. Charlene started their career as a Pharmacy Student at Pharmacie Tinebra in 2014. Charlene then worked as a Hospital Pharmacy Employee at CHU de Saint-Etienne in 2014, 2015, and 2016. In 2015, they also participated in a Pharmacy Program as an Erasmus student at HOSPITAL UNIVERSITARIO INFANTA CRISTINA Y HOSPITAL UNIVERSITARIO DEL TAJO SA, where they conducted interaction studies with Hepatitis C treatments.

From 2016 to 2017, Charlene worked at Sanofi Pasteur, first as a Regulatory Affairs Trainee in Europe and then as a Regulatory Affairs Assistant Manager in the Endemics & New Technologies Franchise. Their responsibilities included coordinating registration and renewal dossiers and responding to questions from Health Authorities.

In 2018, Charlene joined Samsung Bioepis as a Global Regulatory Project Manager in Oncology. Their role involved project management, clinical trial application preparation, and submission to multiple agencies, as well as post-approval activities and regulatory monitoring.

Currently, Charlene is working at Alvotech as a Global Regulatory Lead Delegate, Sr. Manager in GRA Strategy. Charlene is responsible for overseeing all regulatory strategic aspects and providing guidance as a regulatory lead delegate.

Overall, Charlene TEDDE has demonstrated expertise in regulatory affairs, project management, and pharmaceutical quality control throughout their career.

Charlene TEDDE has a Master's degree (MD) in Regulatory Affairs, Health Engineering from the Institute of Industrial Pharmacy of Lyon (IPIL). Charlene also holds a Doctor of Pharmacy - PharmD from Université Claude Bernard Lyon 1. Additionally, Charlene has completed a Business formation in Regulatory Affairs, Health Engineering from emlyon business school. Charlene obtained another degree in Pharmacy, Pharmacist - PharmD, from Université Claude Bernard Lyon 1.