Jacque Johnson
About Jacque Johnson
Jacque Johnson is a Sr. Clinical Site Manager at Bristol-Myers Squibb, overseeing oncology clinical trials and collaborating with various teams to ensure quality and timeliness of deliverables.
Title and Role
Jacque Johnson is a Sr. Clinical Site Manager at Bristol-Myers Squibb. In this role, she collaborates with Protocol Managers and Site Managers across various oncology studies to ensure comprehensive tumor assessment data review and cleaning for selected sites in Asia Pacific and the U.S.
Educational Background
Jacque Johnson studied at Southern Connecticut State University, earning both an M.S. in Counseling/Testing and an MPA in Public Administration. She also attended Cornell College and the University of New Haven, contributing to her diverse educational background.
Professional Experience
Jacque Johnson has been with Bristol-Myers Squibb since March 2005. She is responsible for the management of site activities across all phases of oncology clinical trials, from Study Start-Up through Maintenance and Database Lock. Johnson ensures the timeliness and quality of deliverables through oversight of all Site Management activities conducted by the CRO.
Collaborations and Partnerships
Johnson collaborates with the Ono Partnership/Collaboration team as well as Ono’s CROs. Her responsibilities include providing input on process and procedure documents for the Ono collaboration in the oncology program. Johnson also works across oncology studies with Specialized Services and CTAs to facilitate study start/site opening and manage regulatory document submissions.
Clinical Trials and Protocol Development
In her role, Jacque Johnson participates in the development of protocol standards, CRF/eCRF Design, Data Validation review and selection, and the development and review of ICFs. Her extensive experience in managing site activities and collaborating with multiple teams ensures the success of oncology clinical trials at Bristol-Myers Squibb.