Senior Director, Global Clinical Development (GI Oncology)

- Owns and drives clinical development strategy across given asset indications, aligned to overall asset strategy, Target Product Profile (TPP), and relevant disease area strategy. - May lead the Clinical Development Team(s) for given indication(s) depending on program structure - Provides clinical and disease area expertise to integrated disease area and portfolio and therapeutic level strategies - Represents Clinical as the internal and external authority for the indication/disease area, including regulatory interactions and Business Development support. - Engages cross-functionally with internal leaders and partners with external investigators, key opinion leaders, and patient advocacy groups. - Presents clinical strategy, data, and risk assessments to governance bodies, health authorities, and senior leadership.

- Leads a team of physicians and scientists in the design, execution, analysis, and interpretation of all clinical studies for given asset indication(s) - Ensures studies meet regulatory, quality, medical, and access objectives and are aligned with target label indications. - Ensures high quality, timely delivery of innovative protocols and data packages for CSRs and Regulatory Filings; implements quality assurance plans - Accountable for clinical content and data quality for CSRs, trial documents, regulatory submissions, briefing books, and publications. - Oversees trial progress, proactively identifies and mitigates risk, and provides regular status and risk updates to senior management. - Champions quality, compliance, and GCP adherence across all clinical activities, partnering with Development Operations and Compliance as needed.

- Sets priorities aligned to program objectives and works with Clinical Asset leadership to ensure appropriate budget/resourcing - Attracts, develops, and retains top clinical talent through effective leadership, mentoring, and training. - Fosters a culture of scientific excellence, collaboration, innovation, and accountability.

- Advanced degree in Life Sciences required (PhD, PharmD, MS, RN, MD or related field, MD) - Deep clinical and therapeutic area expertise with advanced knowledge of drug development, competitive landscape, and health authority expectations. - 8+ years of relevant experience, including leadership in the design and execution of multiple clinical trials. - Demonstrated success in people leadership and/or matrix leadership roles.

Cambridge Crossing: $273,900 - $331,907 Madison - Giralda - NJ - US: $244,560 - $296,352 Princeton - NJ - US: $244,560 - $296,352

Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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