Patricia Pretara
About Patricia Pretara
Patricia Pretara is the Associate Director of Regulatory Affairs at Bristol Myers Squibb, with over a decade of experience in the field.
Current Role at Bristol Myers Squibb
Patricia Pretara currently holds the position of Associate Director, Regulatory Affairs at Bristol Myers Squibb. She joined the company in June 2020. In this role, Patricia oversees regulatory strategies and compliance to ensure the company's products meet all regulatory requirements. Her responsibilities include liaising with various stakeholders and regulatory bodies to streamline the approval process for new and existing products.
Previous Experience at Celgene
Before joining Bristol Myers Squibb, Patricia Pretara worked for nine years at Celgene, where she rose to the position of Senior Manager, Regulatory Affairs. During her tenure at Celgene, Patricia was responsible for managing regulatory submissions and ensuring compliance with global regulatory standards. She played a key role in the development and execution of regulatory strategies for several significant projects.
Educational Background
Patricia Pretara studied at Boston University. Her academic background provided a strong foundation for her career in regulatory affairs. The education she received at Boston University equipped her with the skills and knowledge necessary for understanding complex regulatory frameworks and effectively navigating the intricacies of pharmaceutical compliance.
Experience in Regulatory Affairs
Patricia Pretara has over a decade of experience in the field of regulatory affairs. Her career encompasses senior roles at both Celgene and Bristol Myers Squibb, making her well-versed in regulatory strategies, compliance, and project management. Her extensive experience ensures that she brings a wealth of knowledge and a deep understanding of regulatory environments to her current role.