The Sr. Scientist will drive the development and technology transfer of radiopharmaceuticals, managing scientific projects across teams to ensure successful drug product commercialization.

Lead cultural transformation and enhance executive engagement within Medical Affairs. Drive strategic communication, collaboration, and external partnerships while ensuring alignment with corporate priorities.

The Associate Director of Biostatistics collaborates on clinical trial design, manages statistical analysis, and supports regulatory submissions, while mentoring team members.

The DevEx Technical Program Lead will guide technology delivery in the Global Product Development division, leading teams and managing the SPARTAN platform roadmap, while ensuring collaboration and innovation in analytics solutions.

The Data Scientist I will support operational analytics for GPS, developing and implementing models and data pipelines to derive insights for business decision-making.

The Associate Director oversees risk management in clinical trials through analytics and reporting, ensuring data quality and compliance, while collaborating with stakeholders to maintain effective risk strategies.

The role involves architecting and managing data management and analytic capabilities, collaborating with stakeholders to develop data requirements and ensure quality assurance of data assets.

The Associate Director oversees eCOA operationalization for clinical trials, ensuring successful vendor collaboration and addressing study conduct issues while leading continuous improvements and team development.

The Solution Architect will manage Workday Extend applications, ensuring they meet business requirements, develop and maintain applications, and stay updated with new Workday features.

The Senior Manager of Biostatistics oversees clinical study designs, statistical analyses, and regulatory submissions, collaborating with cross-functional teams to communicate results effectively.

The Senior Manager of Analytical AI leads a team in developing and deploying data science and machine learning solutions while collaborating with stakeholders to enhance data-driven decision-making.

The Associate Director role focuses on risk management and monitoring within clinical trials, ensuring compliance and data quality while developing risk oversight strategies and improving processes across the portfolio.

The Key Accounts Manager will develop relationships with key customers, boost BMS brand sales, and execute strategies to drive growth in the Government sector, particularly in Karnataka and Kerala.

The Key Accounts Manager will develop relationships with key government customers, executing KAM strategies and maximizing business opportunities for BMS in the oncology sector.

The Software Engineer I will optimize trials by creating and automating data pipelines, enhancing user interfaces with Tableau and React JS, and collaborating with cross-functional teams.

The Document Coordinator is responsible for managing clinical trial documentation, including collection, compilation, and approval, while collaborating with CROs and internal teams. The role involves maintaining communication with study teams, handling regulatory submissions and overseeing essential documentation throughout the trial phases.

Lead the development of AI-based economic and predictive modeling for healthcare, focusing on HEOR, payer strategies, and collaboration across global teams.

The role involves strategic partnership for medical planning, overseeing project execution, managing budgets, and collaborating across functions to achieve medical objectives.

The Senior Manager will develop trial health status using centralized monitoring, assess clinical trial risks, and lead analytics initiatives.

Manage transactional data operations for BMS, ensuring compliance and efficiency. Lead data analysis and operational initiatives while collaborating with stakeholders.