Shari L.
About Shari L.
Shari L. is a Sr. Clinical Study Manager at Bristol-Myers Squibb with over 30 years of experience in the clinical research industry.
Company
Shari L. is currently employed at Bristol-Myers Squibb, a prominent global biopharmaceutical company. She has been with the company for over 15 years, initially starting as a Clinical Study Manager and eventually advancing to her current role as Sr. Clinical Study Manager. Bristol-Myers Squibb focuses on discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases.
Title
Shari L. holds the position of Sr. Clinical Study Manager at Bristol-Myers Squibb. In this role, she oversees the planning, execution, and management of clinical trials. Her responsibilities include ensuring compliance with regulatory requirements, managing study timelines, and coordinating with various stakeholders to ensure the successful completion of clinical studies.
Education and Expertise
Shari L. graduated from Rutgers University with a degree in Public Health. She has accumulated over 30 years of industry experience in clinical research. Throughout her career, she has held various roles, including data coordination, site monitoring, compliance auditing, and clinical study management. Her extensive experience and educational background have equipped her with the expertise needed to excel in clinical research management.
Career Progression
Shari L.'s career journey began at Covance, where she spent 8 years in multiple roles, including Clinical Studies Assistant and Clinical Site Monitor. She then transitioned to compliance auditing, serving as a Sr. Compliance Auditor at PharmaNet and GE Healthcare. In 2007, she joined Bristol-Myers Squibb as a Clinical Study Manager and was later promoted to Sr. Clinical Study Manager. Her career progression showcases her ability to adapt and excel in various facets of clinical research.
Experience in Compliance Auditing
Before her tenure at Bristol-Myers Squibb, Shari L. gained significant experience in compliance auditing. She served as a Sr. Compliance Auditor at PharmaNet for three years and at GE Healthcare for nearly a year. In these roles, she was responsible for ensuring that clinical studies adhered to regulatory standards and internal policies. Her expertise in compliance auditing has contributed to her comprehensive understanding of the clinical research landscape.