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The Senior Clinical Research Associate will oversee clinical study sites, ensuring compliance with regulations, quality of data, and patient safety while mentoring junior staff and supporting study management activities.

The Senior Director, Resource Management oversees global resource and budget management in Clinical Operations, ensuring alignment of resources with portfolio priorities, while driving data-driven decision-making and optimizing operational efficiency.

The Associate Director will design scalable data architectures using Databricks, focusing on performance, governance, and collaboration to enhance data-driven decision-making. Responsibilities include optimizing data processes, integrating systems, and leading rapid proof-of-concept initiatives.

The Senior Manager, Clinical Supply Chain oversees supply planning for clinical studies, manages vendor relationships, and ensures compliance with regulatory requirements while leading process improvements and team staff.

The Associate Director leads and mentors clinical study managers, ensuring alignment with organizational goals and quality standards while managing study performance and resources.

The Senior Scientist in Clinical Analytics will implement data analytics strategies, deliver insights through advanced analytics, and collaborate with stakeholders to drive business efficiencies and decisions.

The Director of Global Clinical Operations, Compliance oversees compliance activities in drug development, ensuring adherence to regulations, managing quality risks, and guiding teams in clinical trial conduct.

The Director of Clinical Science will lead clinical development programs, ensuring execution aligns with scope, integrity, and timelines, while collaborating across teams and with external partners.

The Manager of Clinical Supply Chain oversees drug supply activities for clinical programs, develops supply plans, manages inventory, and ensures compliance with regulations.

The Senior Clinical Research Associate manages site monitoring to ensure data quality and compliance with clinical study protocols, while training junior CRAs and collaborating with study teams.