Working with Us Challenging Meaningful Life-changing Those aren t words that are usually associated with a job But working at Bristol Myers Squibb is anything but usual Here uniquely interesting work happens every day in every department From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms the lives of patients and the careers of those who do it You ll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams Take your career farther than you thought possible Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment We offer a wide variety of competitive benefits services and programs that provide our employees with the resources to pursue their goals both at work and in their personal lives Read more Key Responsibilities The Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation The Global Trial Acceleration Associate will interact with clinical study sites CROs vendors Country Trial Managers CTM Clinical Trial Monitor CTMo the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration start-up maintenance and close-out of clinical studies As the main point of contact for essential document management ethical and regulatory submission-related activities develops and maintains cooperative working relationships with relevant stakeholders Support outsourcing activities by interfacing with operational teams support groups and service providers for successful selection contracting and execution of outsourced studies while ensuring compliance with regulatory standards ethical practices BMS outsourcing and procurement policies and procedures Initiate and manage start-up documentation activities for global clinical trials Submission of potenti