Associate Director, Corporate Counsel, Europe

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity:

Revolution Medicines is seeking an experienced and business-oriented attorney to manage global supply chain, commercialization and commercial and clinical contracting activities across Europe and other international markets. This role will focus on drafting and negotiating a broad range of commercial agreements, with particular emphasis on supply chain, manufacturing, distribution and vendor services arrangements.

The role will also manage the commercialization readiness for initial European and other product launches, including review of promotional, medical education and disease awareness materials in accordance with applicable EU and national laws, EMA guidance, EFPIA and national industry codes and internal policies as well as  general support across the European Legal team as business needs evolve.

The ideal candidate will bring strong commercial contracting experience within the biotechnology, pharmaceutical or life sciences industry and demonstrate sound judgment, pragmatism and the ability to operate effectively and at times independently in a fast-paced, collaborative environment.

Key responsibilities:

• Draft, review, negotiate and manage a broad range of commercial agreements, including manufacturing, supply, warehousing, transportation, distribution, consulting, technology services and procurement-related agreements.

• Advise on legal, operational, and regulatory risks associated with pharmaceutical supply chain.

• Manage the commercialization readiness activities for initial European and other product launches, including launch-related contracting and operational infrastructure.

• Review and advise on promotional, medical education, and disease awareness materials in accordance with applicable legal and regulatory requirements.

• Partner cross-functionally with the whole Revolution Medicines organization in Europe including Technical Operations, Distribution and Trade, Procurement, Quality, Commercial, Medical Affairs, Regulatory, Clinical, Compliance and Finance teams.

• Provide legal guidance on contract interpretation, liability/risk allocation, risk mitigation, confidentiality, dispute resolution, and related operational matters.

• Develop contract templates, playbooks, and process improvements to drive efficiency and consistency.

• Collaborate across a broad range of legal, operational, regulatory and strategic matters handled by the European Legal team and liaise where necessary with equivalent positions in US and other legal teams.

Required Skills, Experience and Education:

• Law degree from an accredited university and qualification to practice law in at least one jurisdiction.

• 8+ years of relevant legal experience leading commercial contracting, supply chain, manufacturing, commercialization and/or distribution transactions.

• Experience within the pharmaceutical, biotechnology, life sciences or healthcare industries.

• Strong experience drafting and negotiating complex commercial agreements independently.

• Experience leading pharmaceutical commercialization activities and/or launch readiness initiatives.

• Familiarity with EU and international regulatory frameworks applicable to pharmaceutical promotion, supply and distribution activities, including GDP requirements and relevant industry codes.

• Excellent communication, collaboration, drafting and stakeholder management skills.

• Business-oriented mindset with strong judgment and pragmatism.

• Comfortable working in a fast-paced, high-growth, mission-driven environment.

• Proactive, highly organized and able to work independently.

• Excellent drafting and negotiation skills in English; additional European language skills are a plus.

Preferred Skills:

• Prior in-house legal experience within a global biotechnology or pharmaceutical company.

• Experience owning international supply chain operations.

• Familiarity with pharmaceutical commercialization and international distribution models.

• Experience in managing distributor, licensing or commercial partner relationships outside the United States.

• Familiarity with GMP/GDP environments and trade compliance matters.

• Experience with contract lifecycle management (CLM) systems and process improvement initiatives.

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