Kathleen Meyer
About Kathleen Meyer
Kathleen Meyer is a Senior Clinical Site Manager at Bristol-Myers Squibb in New Jersey with extensive experience in clinical research and site management.
Current Role at Bristol-Myers Squibb
Kathleen Meyer currently holds the position of Senior Clinical Site Manager at Bristol-Myers Squibb in New Jersey, United States. As a Senior Clinical Site Manager, she is responsible for overseeing clinical trial sites, ensuring compliance with protocols, and managing study-related training for both sites and internal teams. Her role emphasizes coordination with various vendor teams to ensure the success of clinical projects.
Past Experience at Docs
Kathleen Meyer worked as a Clinical Site Manager at Docs from 2015 to 2016 for a duration of one year. Located in Leopardstown, Dublin, Ireland, her role involved site management activities which likely included maintaining regulatory compliance, overseeing clinical site operations, and ensuring the efficient execution of clinical trials.
Experience at Syneos Health
In 2014, Kathleen Meyer served in a dual capacity as Senior Clinical Research Associate and Site Management at Syneos Health (previously Inc Research/inventiv Health) in Morrisville, North Carolina, United States. Although her tenure was brief, she contributed to clinical monitoring and site management efforts, demonstrating her expertise in data review and protocol compliance.
Long-Term Tenure at Quintiles
Kathleen Meyer had a significant tenure at Quintiles, where she worked from 2005 to 2014 in Durham, North Carolina, United States. Over nine years, she held positions such as Senior Clinical Research Associate and Site Management and Clinical Research Associate. Her responsibilities included clinical monitoring, regulatory compliance, site management, and ensuring the execution of clinical studies aligned with regulatory standards.
Early Career at Pra Health Sciences
From 2000 to 2005, Kathleen Meyer worked at Pra Health Sciences in Raleigh, North Carolina, United States. Serving first as a Regulatory Specialist, then advancing to Clinical Research Associate, and finally as Lead In-house Clinical Research Associate, she gained comprehensive experience in regulatory compliance, project planning, and team development. Her work laid a strong foundation in quality compliance and operational excellence within clinical research.
Educational Background at Rowan University
Kathleen Meyer earned a Bachelor of Arts in Media Studies and Communication from Rowan University. Her academic background provided her with skills in communication and media, which have likely benefited her roles in clinical research through effective communication and training delivery to her teams and clinical sites.
Skills and Expertise in Clinical Research
Kathleen Meyer possesses extensive expertise in clinical monitoring, site management, pharmacovigilance, and regulatory compliance. She has demonstrated the ability to meet project deliverables and timelines effectively, administer protocol training, and manage quality compliance. Her skills encompass team development, relationship management, project planning, budgeting, and tracking, contributing to the successful execution of clinical trials.