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Responsible for designing and implementing data governance capabilities in R&D, collaborating with stakeholders to ensure compliance and optimize data management across clinical domains.

The Clinical Site Contracts Controller analyzes and negotiates site budgets, enhances budgeting processes, identifies cost drivers, and maintains data integrity in a dynamic environment.

The Associate Director, Platform Engineering is responsible for building and maintaining a digital platform, overseeing engineering strategy, compliance, team mentorship, and cross-functional collaboration to ensure platform reliability and innovation.

As a Senior Manager, R&D Data Steward, you will oversee stewardship of Pharma R&D data, ensuring data quality and compliance across the R&D value chain. You will lead a team, operationalize data governance, and drive improvements in data management processes, leveraging automation and cross-functional collaboration to enhance data-driven insights.

Manage and oversee eTMF processes, including system validation, data migration, and process optimization. Collaborate with teams for reporting and improvements while ensuring project deadlines are met.

Lead statistical analyses for Real-World Data (RWD) and Evidence (RWE) studies, oversee programming deliverables, analyze large datasets, and provide statistical consultation for biostatistics projects.

The Senior Manager will oversees clinical development programs, ensuring their execution stays on scope, budget, and timelines, while supporting various functional areas and collaborating with external partners.

Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.

The intern will support analytical development and QC activities, conduct data analysis, and manage QC documents in a fast-paced, collaborative environment.

The Director, Global Regulatory Project Management leads oncology regulatory strategies, ensuring successful global drug submissions, while driving operational excellence and collaboration across teams.