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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.

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.

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 Senior Learning Business Partner in Global Clinical Operations focuses on developing technical and leadership capabilities, designing training programs, and ensuring alignment with regulatory standards.

The Senior Manager in R&D Data Literacy & Monetization drives the strategic utilization of R&D data, transforms datasets into reusable products, and promotes data literacy across the organization, ensuring effective governance and promoting advanced analytics and AI initiatives.

Lead the Central Statistical Monitoring team to oversee statistical design and governance in clinical trials, ensuring data integrity and safety. Develop monitoring indicators, validate models, and communicate findings to cross-functional teams. Provide training and support for audits and inspections, promoting continuous improvement in statistical practices.

The Associate Director manages technology transfer for drug product development, collaborating with various stakeholders to ensure project success and maintaining manufacturing processes.

Support GxP Surveillance through monitoring regulatory requirements, daily screening of updates, and generating reports for regulators. No supervisory role involved.

The Senior Director leads study start-up operations across North America, ensuring rapid site activation, managing budgets, and overseeing regulatory submissions while promoting continuous process improvements and team development.

Lead the Biologics IP team, oversee IP portfolio, provide legal counsel on patent and regulatory matters, and support R&D and commercialization efforts.