Manager I, Global Submission Management - CMC

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Position Summary • Should be pulled from the appropriate Job Description data in Workday, appropriate source per department, or a contractor agreement. • Several top-line sentences in plain text, focused on key accountabilities or duties. • Ideally no more than 75 words. • Avoid internal jargon or acronyms. The Manager, Submission Management supports end-to-end regulatory activities for assigned projects, including leading the preparation and compilation of compliant US IND and marketing complex submissions for global health authorities and supporting continuous improvement initiatives. Position Responsibilities • Should be pulled from the appropriate Job Description data in Workday, appropriate source per department or a contractor agreement. • Typically 5-9 bullet points; each describing a distinct and primary responsibility of the role. • Avoid generic comments such as “works well with others”, etc. Regulatory (IND and Marketing) Submission Management • Collaborate with stakeholders to define eCTD submission strategies and document requirements, ensuring alignment with regulatory standards and project timelines. • Collaborate with teams to drive the execution of the Global Submission Plan. • Track and ensure timely progress of submission components to Health Authorities. Apply risk and critical path management practices. • Execute submission management and publishing activities in the eCTD publishing system for efficient eCTD production and delivery to HA portals. • Lead/represent team in regulatory/submission meetings driving deliverable and publishing timelines. • Lead/participate in department initiatives within scope. Develop/update procedural documentation as needed. • Execute required activities in RIM systems (Veeva RIM) and use availabile tools to generate reports and track submission content. • Coordinate non-eCTD submissions with international teams. Continuous Improvement Initiatives • Drive initiatives that promote innovation and simplify processes to enhance efficienices for BMS teams. • Lead the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information. • Ensure cross functional alignment for IND and marketing applications across projects, studies, and countries, aligning with regulatory standards and best practices. • Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement.

Degree Requirements Required degrees, certifications, and/or licensure relevant to role. BA/BS degree, science / technology field preferred Experience Requirements Minimum number of years of relevant experience expected. 5+ years relevant submissions experience Key Competency Requirements • Proficient knowledge of global regulatory practices, submission guidelines, and requirements; able to identify and resolve issues with support from senior team members • Strong analytical and critical thinking skills for solution development, decision-making, and implementation; generates alternative solutions by weighing risks and dependencies • Effective communication skills in English (written and oral), including presenting complex information and collaborating with non-English speakers • Solid project management abilities: defines objectives, sets priorities, tracks progress, manages resources, and communicates status and risks within