Jobs at Bristol Myers Squibb

Conducts non-interventional real-world data research for international markets, including data-source identification, study design, statistical programming, analysis, interpretation, and dissemination. Collaborates with medical, HEOR, and other stakeholders on protocols, statistical analysis plans, reports, abstracts, and manuscripts. Applies observational research methods, communicates findings, manages complex projects, and supports innovation using R and AI tools.

Leads end-to-end clinical data management for complex trials, including data collection strategy, EDC requirements, data quality reviews, study documentation, vendor oversight, submission-ready datasets, audits, CAPA, and continuous improvement. Mentors data management leads and represents the function on cross-functional and regulatory teams. Requires clinical drug development expertise, EDC experience, FDA/ICH knowledge, project management skills, metrics analysis, and familiarity with NDA, BLA, and MAA submissions.

Leads biostatistical support for clinical development, including trial design, protocol development, statistical analysis plans, regulatory submissions, data interpretation, and health authority interactions. Manages multiple studies, ensures quality and standards compliance, contributes to strategic drug development decisions, presents analyses, collaborates cross-functionally, and mentors team members.

Provide medical accountability and oversight for multiple Phase 1-3 immunology clinical trials. Lead medical monitoring, safety assessments, protocol input, investigator engagement, and clinical strategy. Author clinical content for regulatory submissions and collaborate across cross-functional teams to design and execute clinical development plans.

Leads data science strategy and advanced analytics across drug development programs. Develops statistical, AI, and machine learning models using multimodal clinical and omics data; guides biomarker discovery, precision medicine, trial analysis, and evidence generation. Establishes reproducible pipelines and data quality standards using Python, R, SQL, and cloud platforms. Manages and mentors data scientists while influencing clinical, statistical, and senior leadership decisions.

Lead agile, project-based design and delivery of global commercialization learning programs. Conduct needs assessments, design scalable skills-based pathways, partner with LEAP and vendors, integrate platforms and AI tools, track learner analytics, and drive stakeholder governance, localization, and continuous improvement across Commercial, Medical, Market Access, and Field teams.

Develop and execute commercialisation learning strategies for UKI and Nordics sales teams. Design and deliver training covering disease states, clinical and product knowledge, selling skills, leadership, coaching, and capability development. Partner with cross-functional stakeholders, assess program effectiveness using the Kirkpatrick Model, leverage global learning resources, and manage market-level initiatives. Support first- and second-line sales leader development while driving innovative, technology-enabled learning solutions.

Leads the pooled Agile Strategic Learning Partner team, overseeing people management, portfolio prioritization, capacity planning, project resourcing, operating-model design, quality guardrails, and LEAP delivery partnerships. Establishes agile governance and skills-based resource allocation across global commercialization learning programs. Uses workforce strategy, organizational design, operational data, and emerging AI technologies to optimize learning delivery, track performance, manage vendor inputs, and improve enterprise learning outcomes.

Lead translation of national market access strategy into regional execution across the UK and Ireland. Build a Centre of Excellence, design and deliver training, create market access tools (dossiers, payer decks, budget impact models), generate data-driven regional insights, partner with IHMs and cross-functional teams, and ensure compliance with ABPI and internal governance to improve formulary access and reduce time-to-access.