Regina Little
About Regina Little
Regina Little is a Senior Dossier Specialist at Bristol-Myers Squibb, based in Trenton, New Jersey.
Title
Regina Little holds the position of Senior Dossier Specialist at Bristol-Myers Squibb. In this role, she is responsible for managing and overseeing the preparation and submission of dossiers, which are critical documents for regulatory approvals in pharmaceutical processes.
Company
Regina Little is currently employed at Bristol-Myers Squibb, a global biopharmaceutical company, where she has been contributing since February 1991. The company focuses on discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. Regina is based in Princeton, New Jersey, where she also serves as a Submission Publisher.
Experience at Bristol-Myers Squibb
With over three decades of experience at Bristol-Myers Squibb, Regina Little has accumulated extensive expertise in regulatory submissions and dossier management. Since joining the company in 1991, she has played an integral role in the submission process, ensuring compliance with regulatory requirements and facilitating the approval of new medicines.
Current Role and Responsibilities
As a Senior Dossier Specialist and Submission Publisher at Bristol-Myers Squibb, Regina Little's responsibilities include preparing and managing regulatory documents for submission. Her role is crucial in ensuring that all dossiers meet the necessary standards and are completed and submitted in a timely manner. Her work supports the company's mission to develop and bring innovative drugs to market.
Location
Regina Little is based in Trenton, New Jersey, though her professional activities are centered at Bristol-Myers Squibb’s Princeton office. Her proximity to these locations allows her to effectively collaborate with her team and contribute significantly to the company’s regulatory affairs.