Jobs 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.

Lead statistical programming for clinical trials: produce submission-ready outputs using SAS and CDISC standards, implement ADaM specs and e-submission components, review SAPs, advise stakeholders, mentor/coach programmers, and drive process improvements across cross-functional teams.

Provides medical accountability and oversight for Phase 1–3 oncology clinical trials. Leads medical data and safety review, supports protocol design and execution, assesses benefit-risk, collaborates with clinical scientists and patient safety teams, engages investigators and thought leaders, contributes to health authority interactions, and authors regulatory and clinical study documents.

Provides medical accountability and oversight for Phase 2-3 clinical trials, including medical monitoring, safety assessment, protocol input, investigator engagement, and regulatory document authorship. Leads cross-functional teams, supports study execution, and represents medical expertise in health authority interactions and publications.

Develop and validate SAS programs to create derived analysis datasets and TFLs; prepare electronic submission packages; review SAPs and data presentation plans; partner with vendors and cross-functional teams; independently lead programming assignments and drive GBDS efficiency improvements.

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.

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.

Lead design and execution of early-phase clinical pharmacology trials: draft protocols/ICFs, collaborate on CRFs and data review, author CSRs and regulatory submissions, develop site training and present at investigator meetings, monitor safety and clinical data trends, and partner with KOLs and cross-functional teams.