Jobs at Revolution Medicines

Leads Japan GxP Quality Assurance operations for a pharmaceutical Marketing Authorization Holder. Responsibilities include establishing quality systems and governance, supporting product launches, overseeing external GxP providers and CMOs, managing product release and quality events, reviewing risk and quality metrics, and leading regulatory inspection readiness. Serves as Deputy Quality Assurance Manager and provides independent quality oversight across the product lifecycle.

Leads Japan product quality assurance activities across the pharmaceutical product lifecycle, including launch readiness, product release, quality events, deviations, CAPAs, change controls, complaints, recalls, audits, inspections, GDP activities, and outsourced partner oversight. The role supports Japan MAH operations, quality systems, risk assessments, trend analysis, continuous improvement, and collaboration with global cross-functional stakeholders.

Leads Quality Systems and Compliance for the Japan Marketing Authorization Holder organization. Establishes and improves the QMS, manages deviations, CAPA, change control, training, document management, self-inspection, and inspection readiness. Oversees eQMS processes, GxP compliance, quality metrics, management reviews, regulatory inspection support, and product launch readiness while collaborating globally and building the Japan QA organization.

Leads the strategy, governance, roadmap, and evolution of a global digital experience platform ecosystem. Oversees web platforms, analytics, tagging, consent management, localization, integrations, security, accessibility, vendors, and product launch enablement. Establishes reusable standards and operating models across markets, manages website portfolios and backlogs, evaluates AI-enabled capabilities, and partners with commercial, medical, technology, security, privacy, and agency stakeholders.

Leads pharmacovigilance and safety science activities for Japan, including signal detection, clinical safety oversight, J-RMP development, Japanese package insert maintenance, safety surveillance, and benefit-risk assessment. Collaborates with global and Japan safety, clinical, regulatory, medical, CRO, and external stakeholders while ensuring compliance with Japanese GVP/GPSP regulations and global patient-safety standards.

Oversee Japan safety and pharmacovigilance systems, including administration, user access, data quality, system changes, validation, incident resolution, vendor coordination, documentation, training, and audit readiness. Ensure compliance with Japanese GVP/GPSP requirements and global patient-safety standards while coordinating with global safety, IT, CROs, vendors, and cross-functional stakeholders.

Leads Japan safety operations, including ICSR processing, safety data reconciliation, aggregate reporting, safety agreements, post-marketing pharmacovigilance, audits, inspections, CAPA follow-up, vendor oversight, procedures, workflows, and training. Ensures compliance with Japanese GVP/GPSP requirements while coordinating global teams, CROs, and external partners.

Leads complex cross-functional commercial operations initiatives across the CNE region. Responsibilities include governance, executive and leadership meeting coordination, regional calendar management, internal events, international travel planning, budget tracking, contract and purchasing coordination, office setup, documentation, and stakeholder engagement within a regulated biopharmaceutical environment.

Leads oncology portfolio marketing and product launches in Austria, translating European strategies into locally relevant commercial plans. Oversees brand, omnichannel, customer experience, promotional campaigns, portfolio performance, and cross-functional launch readiness with Field Force, Medical Affairs, Market Access, and Operations. Drives data-driven marketing transformation, stakeholder alignment, customer engagement, and collaboration across European and local teams. Requires extensive oncology marketing leadership, launch management, digital marketing expertise, and willingness to travel within Austria and Europe.

Leads strategic sourcing and supplier strategies across pharmaceutical development, manufacturing, APIs, drug products, and packaging. Responsibilities include sourcing events, supplier negotiations, contracting, risk management, cost optimization, supplier performance, market intelligence, business continuity, executive reporting, and team leadership. Partners cross-functionally with Procurement, Legal, Finance, Quality, and manufacturing stakeholders in a global, matrixed pharmaceutical environment.

Leads congress and event strategy and end-to-end execution across Spain and Portugal. Responsibilities include planning national congresses and internal events, managing vendors, agencies, budgets, logistics, booths, attendee experiences, compliance, transparency reporting, and post-event evaluations. The role coordinates cross-functional stakeholders across Medical, Commercial, Market Access, Compliance, and Marketing while supporting symposia and investigator events and integrating congress activities into broader omnichannel engagement plans.

Leads oncology portfolio marketing and commercial strategy in Switzerland, including product launches, brand development, omnichannel customer engagement, promotional campaigns, and commercial readiness. Coordinates Marketing, Field Force, Medical Affairs, Market Access, Operations, and European teams to translate global strategies into local execution. Owns customer experience, portfolio performance, data-driven marketing transformation, congress activation, and stakeholder alignment while developing agile, technology-enabled marketing capabilities.

Leads global drug supply chain business systems, including planning, inventory, distribution, packaging artwork, serialization, product security, and system integrations. Owns technology roadmaps, implementations, vendors, budgets, data integrity, validation, and regulatory support for DSCSA and EU FMD requirements. Drives AI and automation initiatives, supports product launches and recalls, and manages teams and continuity during supply disruptions.

Leads regional and local market access activities for Germany, identifying reimbursement barriers and executing launch and access strategies for oncology medicines. Builds relationships with health insurers, physicians’ associations, MDK, pharmacies, hospitals, policymakers, and other healthcare stakeholders. Supports hospital listing, NUB applications, reimbursement initiatives, stakeholder education, regional events, policy monitoring, and actionable recommendations for national market access and lifecycle planning.

Leads analytics strategy for the company’s lung cancer portfolio, using claims, EMR, patient, physician, and market data to generate insights for portfolio strategy, launch readiness, commercialization, patient journeys, biomarker testing, segmentation, and competitive assessment. Partners with cross-functional teams, manages analytics vendors, develops dashboards and performance metrics, informs data strategy, and communicates recommendations to senior leadership.

Leads complex cross-functional initiatives supporting CNE commercial leadership and regional operational readiness. Manages governance frameworks, leadership meetings, events, calendars, travel logistics, budgets, contracts, purchasing, office setup, and documentation. Coordinates stakeholders across European affiliates and global functions while ensuring compliance, confidentiality, effective collaboration, and operational excellence.

Leads European HEOR and RWE strategy and execution for oncology assets, including evidence planning, health economic modeling, real-world evidence generation, HTA submissions, pricing and reimbursement support, payer engagement, and value communication. Partners across Medical Affairs, Market Access, Clinical Development, Regulatory, Commercial, and local affiliates while managing external vendors and scientific collaborators. Requires deep pharmaceutical or biotechnology HEOR expertise, oncology experience, European HTA knowledge, 10+ years of experience, and an advanced degree.

Leads U.S. and Canada People Operations service delivery, including employee lifecycle administration, HR data management, payroll inputs, compliance, audits, escalations, and process controls. Manages and develops team members, improves workflows and self-service capabilities, oversees Workday transactions and data quality, supports Canadian operations, and coordinates HR technology and cross-functional projects. Partners with HR, Finance, Payroll, IT, Legal, and other stakeholders to deliver accurate, scalable, and efficient people services.

Leads regional insights and thought leader engagement for pancreatic cancer in Japan. Builds KOL relationships, develops engagement plans, gathers treatment and patient-journey insights, executes speaker and peer-to-peer programs, supports launch readiness, and shares findings with Marketing, Sales, Medical Affairs, and other functions. Manages cross-functional projects, budgets, schedules, vendors, and compliance while supporting brand and customer engagement strategies.

Leads regional insights and thought-leader engagement for pancreatic cancer in Japan. Responsibilities include KOL mapping, relationship building, insight generation, speaker and peer-to-peer program execution, launch readiness, cross-functional collaboration, compliance, vendor and budget management, and team development. Requires oncology pharmaceutical experience, Japanese market knowledge, people management, strong communication skills, and professional Japanese proficiency.