Jason Bruen
About Jason Bruen
Jason Bruen is the Associate Director of Scientific Writing at Bristol Myers Squibb, with extensive experience in medical writing and regulatory documentation.
Company
Jason Bruen currently serves as Associate Director Scientific Writing at Bristol Myers Squibb. His role involves providing advanced scientific writing expertise to clinical teams, ensuring the preparation of high-quality, submission-ready documents supporting regulatory submissions and approvals in key markets.
Title
Jason Bruen holds the title of Associate Director Scientific Writing at Bristol Myers Squibb. In this role, he leads the document strategy and authoring of clear, concise regulatory documents.
Education and Expertise
Jason Bruen studied at Iowa State University, where he earned a Bachelor of Science degree in Engineering Operations from 1996 to 2001. His expertise spans across writing, editing, project management, communication, facilitating, resource assessment, issue resolution, and regulation knowledge.
Background
Jason Bruen has a substantial background in medical and scientific writing, with a career beginning in 2002 at Abbott Laboratories as a Medical Writer (contractor). He advanced through various roles, including Associate Quality Project Manager and Senior Medical Writer, before moving to Celgene. There, he served as Senior Medical Writer, Principal Medical Writer, and Principal Medical Writer II between 2012 and 2021.
Achievements
Jason Bruen has played a key role in authoring complex clinical documents needed for regulatory submissions. His work includes pivotal Phase 3 CSRs, CTD summary documents, pediatric investigational plans, briefing documents, advisory committee brochures, and responses to health authority queries. His efforts support the speed of information during product development, submission, approval, and lifecycle management in the Bristol Myers Squibb pipeline.