Jobs at Revolution Medicines

Leads strategic planning, operational excellence, communications, and enterprise initiatives for the Market Access organization. Translates objectives into measurable plans, manages leadership operating cadences, coordinates KPIs and resources, oversees cross-functional programs, and supports executive decision-making. Partners with Commercial, Medical Affairs, HEOR, Finance, Legal, and Compliance to align market access priorities, improve execution, and support successful product launches and patient access.

Leads U.S. pharmaceutical strategic pricing and provider contracting, developing pricing analyses, financial models, gross-to-net forecasts, contract recommendations, and executive presentations. Oversees GPO, IDN, integrated health system, and government customer strategies while ensuring regulatory compliance. Partners with Finance, Legal, Market Access, Marketing, Forecasting, and Commercial leadership to evaluate access implications, support contract approvals, and prepare oncology pipeline assets for launch.

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.

Lead and scale HR operations across Europe, implementing payroll and benefits frameworks, ensuring compliance with local laws, supporting HRIS/TA system deployments, partnering cross-functionally with Finance, Legal, and global HR, and serving as the central HR operational contact for European employees.

Leads global market research and insights for targeted oncology therapies, translating complex market, disease, competitive, and managed-care data into strategic recommendations. Supports portfolio, lifecycle, clinical development, and commercialization decisions across geographies. Partners with Commercial Development, Clinical Development, Portfolio Management, Medical Affairs, and analytics teams; manages research vendors; communicates findings to senior leadership; and strengthens organizational understanding of market dynamics and product opportunities.

Leads the contract management function, supervising approximately five Contracts Managers and overseeing workload, service levels, CLM adoption, contracting standards, templates, workflows, reporting, training, compliance, and documentation. The role handles complex agreements and escalated matters, mentors staff, drives process improvements, supports audits and controls, and partners with Legal Operations, Procurement, Finance, IT, and business stakeholders in a regulated life sciences environment.

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.

Leads US healthcare compliance strategy and business partnership for a pharmaceutical company preparing for commercialization. Advises Commercial, Medical Affairs, Clinical Development, and other functions on healthcare laws, promotional activities, stakeholder engagements, risk management, investigations, training, monitoring, governance, and corrective actions. Develops policies, controls, compliance work plans, leadership reporting, and risk-based programs while fostering ethical business practices.

The role involves overseeing statistical programming for oncology trials, providing guidance on regulatory submissions, managing cross-functional collaboration, and ensuring compliance with CDISC standards, while also leading programming teams and projects.

The Director of Analytical Development will lead analytical strategies for small molecule AP and drug product development, overseeing regulatory compliance, cross-functional collaborations, and quality management of external partners.

The Associate Director will oversee statistical programming for clinical trials in oncology, manage programming teams, ensure regulatory compliance, and lead project delivery timelines while providing hands-on SAS programming support.

Lead German market access strategy for oncology launches, prepare AMNOG/G-BA dossiers, engage payers/HTA, drive pricing negotiations, collaborate cross-functionally on value demonstration, and support launch readiness and access solutions.

Lead research informatics strategy and delivery to modernize discovery workflows. Drive platform adoption (e.g., Genedata, Benchling), data models, automation, integrations, governance, and user adoption. Partner with scientists, computational teams, IT, and vendors to enable reproducible, high-quality data, advanced analytics, and AI-enabled discovery while managing roadmaps, priorities, and stakeholder engagement.

Lead compliance business partner for US NSCLC commercialization: advise commercial, medical, market access and field teams; conduct risk assessments, reviews, monitoring, audits, and training; develop policies and governance; embed compliance in launch decisions; partner with Healthcare Law; build and mentor compliance staff as needed; promote ethics and continuous improvement.

Provide high-level executive support to the Chief Development Officer by managing complex calendars, travel, meetings, presentations, confidential information, cross-functional coordination, and operational processes to improve organizational effectiveness and execute leadership priorities.

Lead financial modeling and long-range planning for oncology portfolio strategy, business development, and partnerships. Build and maintain P&L, valuation, NPV/DCF models, run scenario/sensitivity analyses, provide financial insights for asset and portfolio decisions, and collaborate cross-functionally on assumptions and prioritization.

Lead cross-functional commercialization project management for an assigned oncology disease area. Drive global launch readiness, lifecycle management, and complex initiatives by coordinating Commercial, Medical, Market Access, Regulatory, Supply, Legal, and Finance. Build project plans, dashboards, governance, risk and dependency management, and drive alignment and execution across stakeholders while contributing to PM tools, templates, and capabilities.

Lead and scale a global privacy program for a clinical-stage biotech. Advise senior leadership on privacy risk, oversee compliance with GDPR/UK GDPR/HIPAA/CCPA, manage cross-border data transfers, incident response, vendor DPAs, DPIAs, and embed privacy-by-design across clinical, R&D, IT, HR, and commercial functions.

Lead and execute G&A business operations and commercialization-readiness initiatives. Manage complex cross-functional projects, drive process improvement, develop project charters, change management, dashboards, and operational tools, and partner with stakeholders and vendors to deliver measurable outcomes.

Lead lung oncology analytics strategy; partner cross-functionally to translate business questions into analyses of patient, physician, claims, EMR, and market data; drive launch readiness, segmentation, forecasting, and KPI/dashboard development; manage external vendors and inform data acquisition and commercialization strategy; communicate insights to senior leadership.