Bristol Myers Squibb

AI Engineer

• As Director, AI Engineering and Enablement you will lead the architecture, design, and implementation of scalable Enterprise AI applications.
• Drive the technical strategy for Gen AI solutions, ensuring robust integration, security, and performance across the organization.
• Architect, design, and build end-to-end GenAI applications.
• Define solution architectures for leveraging cloud platforms (AWS, Azure, GCP) for scalability, reliability, and security.
• Present and propose technical solutions that fit requirements.
• Plan and coordinate project deliveries to ensure timelines and business needs are met.
• Develop core features and infrastructure; write production-grade code in Python, React, and other languages as needed.
• Lead implementation of best software engineering practices (modularity, version control, CI/CD, automated testing).
• Perform code and architecture reviews to ensure robust, maintainable, and high-performing solutions.
• Drive adoption of engineering best practices across the organization.
• Research, design, and implement Agentic AI solutions using frameworks such as LangChain and LangGraph.
• Build autonomous genAI agents capable of reasoning, multi-step workflows, and tool-usage.
• Optimize agent performance, reliability, and compliance for enterprise production. Evaluate emerging AI techniques, tools, and frameworks; make strategic recommendations.
• Collaborate with UX/UI teams to drive adoption and usability of AI applications.
• Maintain and evolve RESTful APIs and microservices architecture.

Director, AI Engineering – Enablement

Therapist

• Support strategic/tactical planning and execution of US Medical Affairs plans
• Represent BMS US Medical Affairs as a therapeutic area expert in both internal and external venues including the US and Global cross-functional teams, clinical sub-teams, and advisory boards / steering committees.
• Represent BMS at professional meetings, congresses, and local symposia supporting thought leader engagement through scientific exchange
• Provide high quality clinical input and review of congress abstracts, posters, presentation slides, manuscripts, educational materials, Investigator Sponsored Research (ISR) protocols, steering committee and advisory board meeting materials, Medical Information response documents, scientific educational grant requests, patient advocacy grant requests, amongst other Medical materials
• Support various Medical Affairs cross-functional working groups
• Collaborate with Medical Affairs field colleagues to define, guide and execute therapeutic regional strategies and tactics with appropriate use of resources

Associate Director, Multiple Myeloma – US Medical Cell Therapy

Director

• Collaborates in design of innovative and efficient clinical trials, including the selection of study population/endpoints to address study objectives, and contributes to project development strategy
• Defends protocols and analysis plans at internal governance reviews and provides independent reviews of complex protocols.
• Independently authors and/or reviews protocol, statistical analysis plan, clinical study reports, associated publications, and other study level documents
• Presents summary data and analyses results, in a clear, concise, complete, and transparent manner
• Provides statistical support and leadership to address health authority requests, publication, presentation, and other public releases of information
• Manages multiple studies to ensure consistency and adherence to standards within an indication or therapeutic area
• Applies extensive knowledge of statistical/clinical trials methodology as it relates to clinical development
• Invests in developing knowledge outside of traditional statistical expertise in the clinical, regulatory and commercial environments with demonstrated application to study design.
• Effectively engages as a matrix team member on project teams, acting as a scientific and strategic partner in the drug development process
• Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverables
• Contributes to external and internal statistical community of practice
• Develops & advises team members
• Effectively communicates the DQS Mission and Vision in a fashion that generates pride, excitement and commitment within DQS.
• Enables a culture of inclusiveness, respect for diversity, compliance with process, and allows for the questioning and challenging of others in a respectful and constructive manner.
• Effectively engages as an employee advocate and management coach/mentor to team members - both internally and externally
• Provides leadership to empower and develop the team. Provides guidance to employees' development plans and carries out performance reviews and feedback. Develops performance metrics for staff.

Director, AI Engineering – Enablement

Associate Director, Multiple Myeloma – US Medical Cell Therapy

Associate Director – Biostatistics