Jobs at Revolution Medicines

Senior finance leader partnering with country and regional leadership to oversee FP&A, statutory reporting, governance, revenue/gross-to-net, and finance operations across Europe Midsize Markets. Drive budgeting, forecasts, decision support, shared-services coordination, audit and compliance, and continuous improvement of finance processes and systems.

Senior finance leader for France affiliate providing business partnership to Country Manager and local leadership. Oversees budgeting, forecasting, P&L, statutory reporting, governance, revenue/gross-to-net, shared-service coordination, audit/tax support, and continuous improvement of finance processes to support commercial execution and launch readiness.

Senior finance leader for the Germany affiliate serving as strategic business partner to local leadership. Responsible for budgeting, FP&A, statutory reporting, governance, gross-to-net, shared-services coordination, financial modelling, audit support, and driving finance process improvements to support commercial execution and regulatory compliance in a life-sciences environment.

Lead global Quality Systems Monitoring & Excellence to ensure QMS governance, inspection readiness, audits, CAPA oversight, KPI/KQI reporting, root cause analysis, and regulatory remediation. Drive process standardization, regulatory intelligence, digital quality tools, and team development to sustain compliance and continuous improvement across the organization.

Lead Switzerland market access strategy for oncology portfolio: develop reimbursement, HTA and pricing submissions; engage payers/HTA bodies; align with regional teams; drive value demonstration, launch readiness, innovative pricing/contracting, and stakeholder engagement to secure patient access.

The Director, Portfolio Omnichannel leads the strategy and execution of HCP engagement in oncology, optimizing customer journeys and driving growth through innovative marketing strategies across various channels.

The Associate Director, Accounting will lead accounting operations, financial reporting, and compliance in Japan, supporting future commercial readiness by developing scalable processes and overseeing financial systems implementation.

Senior leader responsible for defining and executing global GxP compliance strategy across clinical and commercial programs. Oversees inspection readiness, QMS, CSV/eQMS, supplier quality, compliance risk management, KPIs, and cross-functional governance. Advises executive leadership, leads regulatory inspection interactions, and supports product launches, transfers, and global expansion.

Provide pharmacovigilance and medical safety oversight for clinical programs, including signal detection, ICSR review, safety surveillance, risk management, authoring safety sections of protocols/IBs/DSURs, presenting safety summaries, and supporting regulatory safety submissions across product lifecycle.

Lead and scale FP&A for the Japan affiliate: own budgeting, forecasting, management reporting, financial modeling, launch readiness, and decision support. Partner cross-functionally and with global finance to build processes, tools, dashboards, and perform scenario analyses to support commercialization and growth.

Lead commercial packaging supply activities: serve as technical lead for CMOs and suppliers, manage deviations/complaints, author specs and BOMs, support tech transfers, validations, launches, regulatory inspections, and cross-functional continuous improvement to ensure compliant, uninterrupted commercial supply.

Lead global brand strategy and multi-year commercial planning for oncology assets. Translate market, patient, and clinical insights into positioning, messaging, and launch readiness. Drive cross-functional alignment, agency/vendor management, budgeting, and measurement. Partner with Medical Affairs and Market Access to ensure compliant scientific narratives, payer value, and testing strategies. Travel as needed.

Provide in-market legal advice and commercial support to the German affiliate during oncology product launch. Advise on market access, pricing, competition and healthcare law, contracts, litigation, compliance, and cross-functional initiatives. Manage external counsel, legal budgets, and deliver training while partnering with European and global stakeholders.

Lead translational assay strategy and execution to enable biomarker discovery, mechanism-of-action and resistance studies using patient-derived samples, preclinical models, functional genomics, single-cell/spatial and multi-omic approaches. Drive reverse-translation, integrate experimental and clinical/computational datasets, mentor scientists, and partner cross-functionally to inform therapeutic and biomarker strategies.

Lead global serialization and traceability for commercial product launches and lifecycle management. Implement and operate DSCSA, EU FMD, EPCIS data exchange, GS1 registration, aggregation, and partner connectivity. Manage alerts, investigations, onboarding, data governance, SOPs, change controls, packaging artwork approvals, and cross-functional coordination with Supply Chain, Quality, Regulatory, Packaging, Manufacturing, and IT to ensure compliant, scalable serialization operations.

Lead enterprise procurement at a clinical-stage biotechnology company. Build and execute procurement strategy, scale operating model, run strategic sourcing and supplier governance, drive procurement transformation, implement procurement systems and processes, oversee supplier risk/compliance, and mentor a growing procurement team to support R&D, clinical, manufacturing, commercial, IT, and corporate functions.

Serve as subject-matter expert for outsourced stability studies: coordinate and track studies, maintain stability database, author/review protocols/reports, perform trend/statistical analyses, support regulatory CMC filings (IND/NDA/IMPD), partner with quality on investigations/CAPAs, manage sample chain-of-custody, and work cross-functionally to support clinical and commercial stability needs.

The Director of Program Management will lead cross-functional teams in the clinical development of RAS(ON) inhibitors, ensuring efficient execution of the development strategy and managing project risks and stakeholder communications.

The Regional Insights and Engagement Director engages with Lung Cancer KOLs, develops strategies, and collaborates with cross-functional teams to support brand objectives and enhance market strategy.

Lead Computer System Validation and Computer Software Assurance for GxP computerized systems across Information Sciences. Provide technical guidance on FDA 21 CFR Part 11, EU Annex 11, GAMP5 and data integrity, develop validation strategies and deliverables, mentor teams, manage deviations/CAPAs/change controls, support inspections, and drive continuous improvement of risk-based validation and CSA practices.