Phyllis Diener
About Phyllis Diener
Phyllis Diener is the Associate Director, Clinical Trial Management Line Manager at Bristol-Myers Squibb in Lawrenceville, New Jersey, with extensive experience in managing clinical trials and clinical operations.
Title
Phyllis Diener currently holds the position of Associate Director, Clinical Trial Management Line Manager at Bristol-Myers Squibb.
Company
Phyllis Diener is employed at Bristol-Myers Squibb in Lawrenceville, New Jersey. She manages clinical trial operations, focusing on ensuring effective clinical trial management and operation strategies.
Previous Employment
Before joining Bristol-Myers Squibb, Phyllis Diener held various key roles in the pharmaceutical industry. She worked at PRA Health Sciences as a Senior Project Manager, supporting Janssen Pharmaceuticals from 2015 to 2017. In 2014, she served as a consultant in Global Medical Affairs Strategic Operations at The Janssen Pharmaceutical Companies of Johnson & Johnson. Diener's experience also includes a role as Associate Director, Clinical Operations at Daiichi Sankyo from 2010 to 2014 and a decade-long tenure at sanofi-aventis as Senior Director, Clinical Operations from 2000 to 2010.
Education and Expertise
Phyllis Diener has a Bachelor of Science in Medical Technology from Fairleigh Dickinson University. She is also certified in Clinical Laboratory Science/Medical Technology/Technologist from Morristown Hospital School of Medical Technology. Her extensive expertise spans managing clinical trials across therapeutic areas, including cardiovascular, allergy, respiratory, infectious disease, oncology, dermatology, CNS, diabetes, hematology, immunology, and orthopedics.
Roles and Responsibilities
At Bristol-Myers Squibb, Phyllis Diener participates as a representative on SOP Committees and contributes to SOP writing. She serves as an alliance management liaison to CRO counterparts in joint operating committees. Diener's roles include personnel management, strategic planning, and performance management. Additionally, she oversees CRO/vendor activities and reviews clinical operations processes for efficiency and quality. She advises corporate management on clinical operations' tactical and strategic issues and ensures project management within contracted timelines, budget, and quality standards.