Karen Larkin

Karen Larkin is currently serving as the Associate Director, Documentation Quality Lead / Global Process Lead (CSRs) at Bristol Myers Squibb. In this role, she is responsible for overseeing documentation quality and ensuring compliance with global standards within the organization. Her expertise lies in project management and regulatory affairs, particularly in the healthcare industry.

Throughout her career, Larkin has held significant positions that have contributed to her extensive experience in clinical study protocols and documentation processes. Her background includes a focus on improving operational efficiencies and maintaining high-quality standards in documentation practices, which are crucial for regulatory compliance in the pharmaceutical sector.1

Larkin is based in Wilmington and has built a professional network that reflects her extensive experience in the industry, as indicated by her active LinkedIn profile.1