Tammy L Davis
About Tammy L Davis
Senior Manager, Regional Clinical Operations at Bristol Myers Squibb
Tammy L. Davis is currently serving as the Senior Manager for Regional Clinical Operations at Bristol Myers Squibb. In this role, she oversees the operational aspects of clinical trials including vendor management and coordination with Clinical Research Associates (CRAs). Her extensive experience in the pharmaceutical and clinical research industries informs her management strategies and ensures the successful execution of clinical trials.
Previous Roles at Celgene
Before joining Bristol Myers Squibb, Tammy held two important positions at Celgene. From 2017 to 2020, she worked as the Associate Director of Clinical Trial Management. Prior to this, she was a Senior Study Manager from 2010 to 2017. Both roles were home-based in Wilmington, NC, and involved overseeing clinical trials from start-up to close-out, ensuring that they met regulatory and company standards.
Experience at Abraxis BioScience and PPD
Tammy's career includes a stint as a Clinical Trial Manager at Abraxis BioScience from 2009 to 2010. Before that, she held various roles at PPD from 2003 to 2009, progressing from CRA/SR. CRA to Principal CTM and Project Manager in Wilmington, North Carolina. This diverse range of responsibilities allowed her to gather significant expertise in clinical trial management and operations.
Background in Clinical Research
Tammy L. Davis has over 20 years of experience in the clinical research industry. She has worked for both Global Contract Research Organizations (CROs) and Global Pharmaceutical Companies. Her roles have encompassed managing Phase I-IV clinical trials, vendor management, and line management of CRAs. This extensive background has provided her with a comprehensive understanding of the clinical research field, allowing her to effectively oversee complex projects.
Vendor Management Expertise
Tammy's expertise extends to vendor management across various services required in clinical trials. She manages Central Labs, Specialty Labs, Interactive Voice Response Systems (IVRS), Central Imaging, Central ECG, and Central Radiology. Her role involves ensuring that all these services are coordinated effectively to support the smooth operation and success of clinical trials.