The Senior Manager, GMP Quality oversees QA in drug development, collaborating with teams on compliance, process validation, and managing quality oversight for products.

The Senior Project Coordinator ensures successful project execution for the US Commercial Field teams, coordinating logistics and supporting field events, meetings, and travel planning. The role requires strong organizational skills, stakeholder collaboration, and the ability to manage multiple tasks.

The Senior Manager, Corporate FP&A will manage budgeting and forecasting for Corporate and Research functions, develop financial reporting, partner with research leadership, and lead financial analyses and process improvements.

Manage CMC project management activities for pipeline compounds and commercial products, drive project readiness, and coordinate cross-functional teams for regulatory submissions and launches.

Assist the Quality Assurance team with compliance, documentation, and quality control processes while gaining experience in a regulated biotech environment.

The IS R&D Intern will support the R&D Information Operations team in managing regulated electronic systems, providing insights into system governance and cross-functional collaboration. The role emphasizes learning and communication over technical execution, ideal for students in STEM fields.

The Senior Safety Scientist provides safety science and pharmacovigilance support for clinical studies, including risk management, medical review, and safety oversight, ensuring compliance and collaboration across teams.

As an intern, you'll synthesize compounds, execute experiments, use analytical instruments, and present research findings while collaborating with chemists.

The Director of Employee Engagement will lead and develop global culture and engagement strategies, overseeing programs for employee onboarding, recognition, and satisfaction, while advising senior leadership on analytics-driven decisions to enhance employee experience and organizational effectiveness.

Responsible for SEC reporting, SOX compliance, and technical accounting. Will prepare financial statements, ensure compliance, and support audits.

The Director of Program Management at Revolution Medicines will lead cross-functional teams, manage project risks, and streamline processes to support drug development in RAS-related cancers.

The Director of Biostatistics leads statistical support for clinical development, collaborates on studies in oncology, and provides expertise in regulatory submissions and data interpretation.

The Senior Manager, Data Product Owner will define the data product roadmap, manage commercial data integration, and support launch readiness through actionable insights and collaboration with cross-functional teams.

The Associate Director leads outsourcing for clinical trials, manages vendor relationships, negotiates contracts, oversees budgets, and ensures compliance with service levels and performance metrics.

The Director of Marketing will develop and execute marketing strategies for RAS(ON) programs, collaborate with teams, and lead promotional activities, focusing on lung cancer launches.

Oversee the global data product strategy in precision oncology, leading data product management to support research, clinical development, and commercialization. Foster collaboration across functions and leverage data-driven insights for operational and commercial impact.

The role entails architecting and building enterprise data and AI platforms, collaborating with teams on scalable solutions, and implementing best practices across cloud and data infrastructures.

The Senior Director, Compliance will lead enterprise-wide compliance efforts, advising on corporate governance, risk management, and ensuring alignment with relevant laws and regulations in a growing multinational biotech company.

The Director of Global Marketing will lead the global brand strategy for a key oncology product, partnering across functions to execute commercial plans and ensure launch readiness, while managing budgets and compliance requirements.

Assist in managing global CRM ecosystem, gather requirements, maintain strategic CRM roadmap, participate in user acceptance testing, and create training materials.