Susan Lings
About Susan Lings
Susan Lings is a Clinical Site Manager with over two decades of experience in the pharmaceutical and clinical research industry.
Title
Susan Lings holds the position of Clinical Site Manager, leveraging her extensive experience in managing clinical sites across various companies in the pharmaceutical industry.
Education and Expertise
Susan Lings graduated from Cranfield University, where she obtained a Master of Science degree. Her specialized education has provided her with the foundational knowledge required for the complex and regulated field of clinical research and trial management.
Background in Clinical Trial Administration
Susan Lings has a robust background in clinical trial administration that dates back to the early 1990s. Starting her career at Hoechst Marion Roussel, Susan gained vital experience during a vibrant period of industry changes and mergers, which contributed to her deep understanding of the regulatory and operational aspects of clinical trials.
Experience at Hoechst Marion Roussel
From 1992 to 2000, Susan Lings worked at Hoechst Marion Roussel as a Clinical Trial Administrator (CTA). This role spanned eight years, during which she witnessed and adapted to significant industry transformations, ensuring compliant and efficient trial operations.
Career at Bristol-Myers Squibb
Susan Lings continued her career at Bristol-Myers Squibb, where she took on the role of Clinical Site Manager. Her work at one of the leading global pharmaceutical companies further solidified her expertise in managing clinical sites, overseeing various clinical trials, and ensuring adherence to stringent regulatory standards.