Teams 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.