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Lead analytical chemistry activities for small molecule development, collaborating across project teams to overcome challenges and develop strategies.

The Senior Manager is responsible for compliance oversight, managing investigations, root cause analysis, and implementing CAPAs while ensuring adherence to GCP standards.

Lead in design, conduct, and interpretation of pathology studies, guiding drug development, and collaborating with multidisciplinary teams. Consider regulatory submissions and promote innovative imaging and diagnostic methods.

The Associate Director leads biostatistics efforts in clinical trials, manages team members, authors statistical plans, and collaborates cross-functionally while ensuring quality and compliance with regulatory standards.

The Senior Director, Market Enablement will lead initiatives to enhance kidney product access, collaborate with various stakeholders, and drive market transformation efforts.

The Director of Master Data Management will lead the MDM strategy and operations, focusing on Customer, Supplier, and Product domains. Responsibilities include modernization of data systems, overseeing AI integration, and managing a high-performing team.

The Director leads the GxP training strategy, overseeing governance and compliance within the Quality Management System, while partnering with leadership for effective training solutions.

The Associate Director will provide commercial insights through market research and analytics to inform strategic decisions in Vertex's biopharma products, particularly in kidney disease.

Lead strategic and operational clinical pharmacology activities across programs, develop clinical pharmacology plans, guide PK/PD analyses and modeling, oversee clinical studies and regulatory documents, mentor staff, and support hiring.

The Associate Director will develop and execute digital marketing strategies for healthcare professionals, ensuring compliance and leveraging digital tools to enhance engagement and communication.