Jobs at Revolution Medicines

The role involves developing forecast models for oncology products, collaborating with teams, and communicating assumptions for strategic decision-making across the organization.

Lead and grow the contracts function, managing attorneys and contracts professionals, shaping enterprise contracting strategy, implementing and optimizing CLM systems, maintaining stakeholder relationships, and drafting, negotiating, and advising on a broad range of life-sciences agreements including clinical trial, CRO, supply, NDA, consulting, MSAs, SOWs, and sponsored research agreements.

Lead HEOR/RWE strategy and execution for NSCLC assets, align with Medical Affairs and cross-functional teams, generate global real-world and economic evidence, engage payers/HTA and external partners, communicate value to stakeholders, and shape access strategy and evidence generation.

Lead portfolio analytics, governance, resource and cost management for PDM. Drive cross-functional planning, reporting, scenario modeling, and executive communications. Support budgeting, strategic initiatives, and operational excellence to improve prioritization, capacity management, and decision-making across discovery, development, and commercial programs.

Lead R&D informatics across Research to Clinical: own systems, implement COTS and bespoke tools, build AWS/Databricks pipelines and apps, maintain backlog and value proposition, support GxP validation, collaborate with scientists, and apply AI-forward development and business analysis.

Lead and execute capability-building projects for Development & Clinical Sciences. Design deployable tools and workflows, manage delivery and change adoption, track metrics and drive continuous improvement, and partner with leaders and functional teams to embed scalable processes.

Lead development and execution of Netherlands market access, pricing and reimbursement strategies for oncology portfolio. Prepare HTA/value dossiers, negotiate with payers and authorities, align local strategy with regional teams, build payer relationships, design pricing/value-based contracts, monitor policy, support launch readiness and provide market access insights to clinical, medical and commercial teams.

Lead Netherlands commercial strategy and execution for oncology portfolio. Build and manage country commercial organization, oversee launch readiness, align cross-functionally (Medical Affairs, Market Access), drive demand generation, forecasting, and stakeholder engagement, and monitor market dynamics to optimize performance.

Lead and build a European healthcare compliance function: develop and implement region-specific compliance programs, manage a team, advise commercial and medical activities, conduct risk assessments, training, monitoring, investigations, and partner with global Compliance and cross-functional leaders to support product launches and ensure regulatory and industry-code adherence.

Lead Austria market access strategy for oncology portfolio: shape reimbursement and pricing, prepare HTA/value dossiers, engage payers and HTA bodies, negotiate pricing, support launch readiness, provide local access insights to regional teams, monitor policy, and drive value-based contracting and stakeholder engagement to secure patient access.

Lead Austria commercial strategy and execution for oncology portfolio, build and manage the local commercial organization, drive launch readiness, collaborate cross-functionally with Medical Affairs and Market Access, generate field insights, manage forecasting and budgeting, and ensure stakeholder engagement and performance monitoring across pre-launch to post-launch.

Lead commercial launch and country build-out for Belgium & Luxembourg: develop and execute country strategy, manage P&L and budgets, hire and lead cross-functional team, oversee market access, pricing, regulatory/compliance, distributor selection and contracts, and set launch and financial performance metrics.

Lead development and execution of access strategy and non-clinical positioning for the NSCLC portfolio. Build and manage an Access Marketing team, create payer- and channel-tailored value messaging, drive launch readiness, and align cross-functionally with Brand, Medical/HEOR, Regulatory, Compliance, and field teams to inform evidence and commercialization plans.

Lead commercial and operational expansion in the Netherlands: develop and execute pre-launch and launch plans, manage country P&L and budget, build and lead the country team, ensure market access, pricing and compliance, negotiate distributor contracts, and establish governance, risk management, and SOPs.

The Senior Director, Commercial Lead, UK defines and executes the local commercial strategy for oncology products, ensuring alignment across key functions and driving launch performance.

Lead and optimize global GxP document control and eDMS/eQMS operations. Manage document change controls, workflows, migrations, SOPs, and KPIs. Serve as Veeva QualitySuite SME, support inspections and audits, drive process improvements, training, and cross-functional governance to ensure regulatory compliance and operational excellence.

Lead Cancer Pharmacology and Translational Research to inform candidate selection, IND-enabling studies, PK/PD, efficacy, combination strategies, and biomarker plans. Build and mentor teams, oversee preclinical CRO operations, and integrate large-scale preclinical and clinical datasets with AI/ML and modern data infrastructure. Drive cross-functional collaborations, external partnerships, scientific communications, and strategic disease-area decision making to accelerate oncology drug development.

Lead development and execution of market access strategy and non-clinical value propositions for NSCLC portfolio. Build and coach an Access Marketing team, drive launch readiness, create payer- and managed-care-tailored value messaging, and partner cross-functionally with Brand, Medical/HEOR, Regulatory, Compliance, and field teams to support product lifecycle access.

Lead design, delivery, and continuous improvement of GxP training and curricula, manage companywide training programs in Veeva/eQMS, evaluate training effectiveness, create learning content, develop SOPs and work instructions, and partner cross-functionally to ensure regulatory compliance and inspection readiness.

Lead global finance launch and interim market controllership for new international entities. Develop and maintain launch playbooks, govern processes and controls, design operating models, run reporting and business review processes, and partner with Technical Accounting, Corporate Accounting, SEC, and cross-functional teams to ensure compliant, scalable finance operations.