Associate Director Global Clinical Scientist

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 careers.bms.com/working-with-us.

Director, Global Clinical Scientist 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 rich in diversity. 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 careers.bms.com/working-with-us

Position Summary The Director, Global Clinical Scientist is a member of the Late Clinical Development Function which provides the scientific expertise necessary to design and deliver clinical studies and programs with high quality and urgency.

• Individual contributor role providing support across program(s)
• Serves a key role in the implementation of the Global Clinical Development Strategy for the assigned book of work within an asset and/or indication(s). This includes serving as a subject matter expert and having the capability to represent the CS group in cross-functional initiatives
• Ensures consistency across studies within an asset and/or indication
• Provides support for clinical studies within the assigned asset or indication
• Provides input to strategic discussions and development of clinical development plans (CDPs)

Key Responsibilities

• Serve as a subject matter expert for the development, conduct and regulatory submission of clinical studies including but not limited to
• Protocol development
• Clinical data review
• Data interpretation; review and validation of CSRs
• Regulatory requirements and documents (e.g., IB, submissions, etc)
• Site/KOL engagement strategies and implementation
• Harmonization of standards across programs and/or indications (e.g. data standards, programming specifications, statistical analysis plans)
• Ensure lessons learned are communicated across teams and ensure alignment so that unnecessary amendments are avoided and to align with asset/TA-level protocol elements
• May serve as Trial Lead for complex clinical studies
• May present data/information to internal and external stakeholders including investigators and study staff
• Independently, proactively, and consistently develop, enact, and share best practices
• Clinical oversight of study data, specifically, leverages best practices to guide the CS team(s) in
• understanding interdependencies of CRFs
• data conventions/ rules
• data review tools and visualizations; collaboration with DM and Programming
• Se