Sean R. Doyle, MSc
About Sean R. Doyle, MSc
Sean R. Doyle, MSc, is a Global Trial Manager at Bristol Myers Squibb in Lawrenceville, New Jersey, with extensive experience in clinical research and trial management.
Title at Bristol Myers Squibb
Sean R. Doyle is currently the Global Trial Manager at Bristol Myers Squibb. Based in Lawrenceville, New Jersey, he has been leading global clinical trials since June 2020. In this role, he utilizes his strong project management and organizational skills to ensure clinical research protocols are executed successfully and on time.
Previous Experience at Avid Radiopharmaceuticals
Sean R. Doyle worked at Avid Radiopharmaceuticals for six years. From 2017 to 2020, he held the position of Clinical Trial Manager in Philadelphia, PA. Before this role, he served as a Clinical Research Associate II from 2014 to 2017, also in Philadelphia. At Avid, Doyle gained valuable experience in clinical trial management and research.
Educational Background
Sean R. Doyle holds a Master of Science in Clinical Research Organization and Management from Drexel University, which he earned from 2011 to 2013. Additionally, he has a Bachelor of the Arts in Psychology from The Pennsylvania State University, completed between 2002 and 2006. His educational background provides a strong foundation for his roles in clinical research and trial management.
Professional Role at Bristol Myers Squibb
In his role as Global Trial Manager at Bristol Myers Squibb, Sean R. Doyle serves as the primary operational contact for clinical research protocols. He coordinates the development of protocol-level documents and plans for clinical trials. Doyle leads a global team, employing his strong interpersonal and influencing skills to foster collaboration and efficiency. He addresses and manages obstacles to ensure the smooth progress of the trials, utilizing effective oral and written communication skills.
Early Career and Positions
Sean R. Doyle's early career includes various positions in clinical research. He worked as a Clinical Research Associate at Luitpold Pharmaceuticals from 2012 to 2014 in Norristown, PA. Before that, he was an In-House Clinical Research Associate II at PRA International in 2012 for seven months in Horsham, PA. From 2009 to 2012, he served as an Operations Specialist at ClinForce / Merck & Co., Inc in Ambler, PA. Doyle began his career as a Clinical Project Assistant at PPD from 2008 to 2009 in Blue Bell, PA.