Teams at Bristol Myers Squibb

Provides medical accountability and oversight for Phase 1–3 rheumatology clinical trials. Leads medical data and safety review, contributes to protocol and clinical plan development, supports benefit-risk assessments, and partners with clinical scientists and safety teams. Builds investigator and thought-leader relationships, provides scientific education, supports health authority interactions, and authors clinical and regulatory documents. Requires an MD, at least five years of industry or clinical trial experience, drug development expertise, and strong leadership and communication skills.

Leads statistical programming strategy and delivery for clinical trials and regulatory submissions. Develops and validates SAS programs, ADaM datasets, tables, figures, listings, and e-submission components; reviews analysis plans, manages technical risks, improves programming processes, and mentors team members. Collaborates with biostatisticians, data managers, clinical scientists, and cross-functional stakeholders throughout the drug development lifecycle.

Lead quality and compliance efforts for global clinical trials, executing risk management programs, and fostering a culture of quality excellence. Responsible for identifying business risks and managing cross-functional teams.