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. At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, cell therapy, immunology, Neuroscience, and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. Position Summary The Senior Director of Real-World Evidence Biostatistics plays a pivotal role in leading and overseeing the strategic direction and execution of statistical and real-world evidence initiatives within the organization. This key leadership position involves providing guidance and expertise in statistical methodologies, study design using real-world data to facilitate and support development and regulatory interactions of pharmaceutical products. The Senior Director collaborates closely with cross-functional teams to drive innovation, optimize trial design, and leverage real-world data to support evidence generation and decision-making. Additionally, the role involves representing the organization in interactions with regulatory agencies, fostering a culture of excellence and continuous improvement within the Global Biometrics and Data Sciences, and serving as a thought leader in the field of real-world evidence. Key Responsibilities Provide strategic leadership in the design, execution, and analysis of real-world evidence studies Lead efforts to enhance the utilization of real-world data for evidence generation and decision-making purposes Represent the organization at conferences, forums, and industry events to showcase expertise and thought leadership in biostatistics and real-world data Manage resources and budget to ensure company resources are allocated according to the development needs and priorities Create effective processes related to RWE and ensure consistency and adherence across therapeutic areas and projects Key contributor to Clinical Development Plans, submissions, and post-submission strategies / preparation / defense as needed Represent the company in interfaces with regulatory agencies globally Engage effectively as a matrix team member on high-level development teams and serve as a scientific and strategic partner Seek and establish new collaborations with cross-functional teams for RWE objectives Enable a culture of inclusiveness, respect for diversity, compliance with process, and constructive questioning and challenging of others Leadership and Development Provide leadership to empower and develop the team, guiding employee development plans, conducting performance reviews, and developing performance metrics for staff. Qualifications & Experience PhD or MS (12+ years’ experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience Proficiency in scientific computing / programming (SAS, R or Python) and implementation of advanced statistical analysis Extensive experience in real-world data within the pharmaceutical or CRO industry, demonstrating leadership and strategic thinking In-depth knowledge of statistical methodologies, clinical trial design, and real-world evidence generation, with a focus on optimizing study design and data analysis A commitment to continuous learning and professional development in the field of real-world data Experience in preparing and participating in global regulatory agency interactions Excellent collaboration, organizational / leadership abilities, and interpersonal skills At least 5 years management (direct or matrix) experience preferred Additional Information We promote an inclusive culture, diversity in clinical trials, and shared values of passion, innovation, urgency, accountability, inclusion, and integrity. Our work environment varies by role, including onsite, hybrid, and remote options, with accommodations available for disabilities. We prioritize health and safety, recommending COVID-19 vaccination and boosters. We consider qualified applicants with arrest and conviction records in accordance with applicable laws. All data related to applications are handled per privacy policies and regulations. #J-18808-Ljbffr