Jobs at Revolution Medicines

Lead and provide technical oversight for statistical programming across early and late-phase oncology trials. Produce and QC analysis datasets, tables, listings, and figures; ensure CDISC and regulatory submission compliance; manage vendors/CROs; mentor team members and support submission-related activities and regulatory standards adherence.

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.

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 pipeline and product communications for RAS(ON) inhibitors or tumor types across clinical development, regulatory milestones, and pre-launch. Translate complex clinical data for scientific, medical, patient, and media audiences; coordinate global affiliate execution; manage agencies/vendors; support regulatory, market access, patient advocacy, congresses, publications, earned media, and performance tracking.

The role involves developing and validating quantitative systems pharmacology models, performing simulations, and collaborating across teams to support oncology R&D.

The Senior Manager, GMP Quality oversees quality assurance operations, including compliance, testing, and validation processes for drug development and manufacturing, while leading cross-functional teams.

The ERP Systems Senior Manager leads the configuration and management of NetSuite OneWorld to support global operations, ensuring compliance, optimizing financial processes, and maintaining system integrity while collaborating with Finance and IT teams.

The Associate Principal Statistical Analyst leads statistical programming for oncology clinical trials, manages deliverables, and ensures compliance with regulatory standards, using SAS programming to support analysis datasets and oversee contractor teams.

The Senior Program Manager will lead Companion Diagnostics development activities, ensuring alignment across teams and driving execution of strategies for oncology therapies.

The Senior Manager drives enterprise technology initiatives, ensuring projects align with business goals, manage complex requirements, and comply with regulations. Responsibilities include project oversight, stakeholder partnership, and risk management within pharmaceutical development.

The Senior Manager, GMP Quality is responsible for leading operational GMP QA support in clinical drug development, ensuring compliance, and managing quality systems for clinical batch activities.

Lead design and scaling of a company-wide digital platform: build reusable platform capabilities, reference architectures, shared services, and developer enablement. Define trustworthy AI and agentic engineering practices (RAG, LLM integration, agent orchestration), establish security/observability/CI/CD standards, and coach/mentor senior engineers. Drive governance, onboarding, and measurable adoption of platform patterns to accelerate secure, production-ready digital products across Information Sciences, R&D, and business domains.

Provide pharmacovigilance and safety science support across clinical development. Oversee safety surveillance and medical review of ICSRs, perform signal detection and risk management, prepare safety content for protocols, IBs, ICFs, DSURs and regulatory submissions, present safety summaries, and collaborate with cross-functional teams to maintain product benefit-risk profiles.

Provide strategic healthcare compliance counsel to support product commercialization, advising on laws/regulations, reviewing promotional materials, conducting risk assessments and investigations, developing training, and partnering cross-functionally to implement compliance programs and reporting.

Serve as the DMPK representative on cross-functional drug discovery and development teams. Design and execute in vitro and in vivo metabolite identification and profiling studies, characterize metabolites for MIST and regulatory strategy, perform mechanistic enzyme kinetics studies, support characterization of degradation products, author DMPK regulatory sections, and collaborate across discovery, clinical pharmacology, medicinal chemistry, toxicology, and development.

The Associate Director leads Research operations, translating strategy into actionable plans, enhancing operational efficiency, and driving cross-functional alignment to improve Discovery outcomes.

The Senior Director will lead global oncology marketing efforts by developing strategies, driving commercial execution, and collaborating cross-functionally for product launches and brand management.

This role involves leading biostatistics for clinical programs, providing statistical support for study designs, collaborating across teams, and ensuring compliance with regulatory requirements. The candidate will drive department initiatives and support publications and submissions, requiring extensive experience in oncology trials.

The Executive Director leads global oncology marketing, driving commercial strategy, launch planning, and cross-functional collaboration. This role includes developing brand strategies, managing vendors, and executing impactful global campaigns, all while providing leadership and insights to maximize commercial value.

The Payroll Manager ensures accurate payroll processing, compliance with regulations, oversees audits, supports equity compensation, and mentors payroll professionals.