Anita Sučić
About Anita Sučić
Anita Sučić is the Associate Director of European Regulatory Procedure Management at Bristol-Myers Squibb, with over 15 years of experience in regulatory affairs and procedure management within the pharmaceutical industry.
Current Position at Bristol-Myers Squibb
Anita Sučić currently serves as the Associate Director of European Regulatory Procedure Management at Bristol-Myers Squibb. Based in Brussels, Belgium, she is responsible for overseeing regulatory procedures within the European market. Her role involves managing cross-functional teams and ensuring compliance with European Union regulations. She plays a critical part in the regulatory approval process for various pharmaceutical products.
Previous Roles at Bristol-Myers Squibb
Before becoming Associate Director, Anita Sučić held multiple roles at Bristol-Myers Squibb, including Regulatory Manager and Senior Regulatory Specialist. From 2017 to 2018, she served as the Regulatory Manager of European Regulatory Procedure Management in Brussels, Belgium. Prior to that, from 2015 to 2017, she worked in New York, USA, as a Senior Regulatory Specialist, where she focused on European regulatory procedures.
Experience at Keyrus Biopharma and Agency for Medicinal Products and Medical Devices
Anita Sučić's career includes a period as a Senior Regulatory Affairs Associate at Keyrus Biopharma in 2014-2015. Before this, she was affiliated with the Agency for Medicinal Products and Medical Devices in Croatia, holding positions such as Head of Regulatory Affairs Department, Head of European Affairs, and Expert Associate and Acting Spokesperson. Her work there spanned from 2005 to 2014.
Educational Background
Anita Sučić holds a Master's degree and a Doctorate (Doctor of Philosophy) from the University of Zagreb/Sveuciliste u Zagrebu. She completed her Master's degree from 1998 to 2002 and her Doctorate from 2002 to 2007. Additionally, she studied at Supera Business School from 2008 to 2009, further advancing her academic and professional qualifications.
Industry Experience and Contributions
With over 15 years of experience in regulatory affairs and procedure management within the pharmaceutical industry, Anita Sučić has played a pivotal role in regulatory approvals for several major pharmaceutical products. Her extensive experience includes managing cross-functional teams and collaborating with regulatory agencies across Europe. She has contributed significantly to the development and implementation of regulatory strategies ensuring compliance with European Union regulations. Her scientific research background further enhances her expertise, bridging the gap between research and regulatory affairs.