Director, Pipeline & Product Communications

Job description

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

The Opportunity:

The Director, Pipeline & Product Communications will lead pipeline and product communications strategy and execution for one or more RAS(ON) inhibitors or tumor types, supporting programs from early clinical development through regulatory milestones and pre-launch readiness. This role is responsible for shaping how tumor-specific pipeline and product narratives are communicated to external stakeholders, including scientific and medical audiences, patients and advocates, and industry media.

Reporting to the Senior Director, Pipeline & Product Communications, this role will partner closely with cross-functional teams, including R&D, Medical Affairs, Regulatory, Commercial, Market Access, Patient Advocacy, Legal, and Corporate Communications, to ensure clear, consistent, and differentiated communications for the assigned tumor area.

This is a high-impact role for a communications professional who combines scientific fluency with strong executional rigor and cross-functional collaboration.

Key Responsibilities:

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Own pipeline and product communications for one or more RAS(ON) inhibitors or tumor types, ensuring clear differentiation, scientific credibility, and alignment with overall corporate and pipeline strategy.

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Lead communications execution for clinical milestones, including data readouts, abstracts, presentations, and major medical congresses.

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Partner with R&D and Medical Affairs to translate complex clinical and scientific data into clear, compelling external messaging tailored to the tumor-specific audience.

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Partner with affiliate communications teams in ex-U.S. markets to align on communications strategy and ensure globally consistent, locally relevant execution across key pipeline and product milestones.

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Support regulatory and pre-launch communications, including trial initiations, regulatory submissions, approvals, and launch readiness activities.

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Execute disease awareness and patient advocacy communications in partnership with Patient Advocacy, ensuring responsible education and inclusion of patient voice.

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Support communications related to value, access, and product-specific issues, in coordination with Market Access, Legal, and Corporate Communications.

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Contribute to scientific and medical thought leadership efforts, including congress presence, publication support, speaker positioning, and external engagement.

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In partnership with Corporate Communications, support earned media efforts for industry, trade, and scientific publications tied to tumor-specific milestones.

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Manage agency partners and external vendors supporting the tumor-specific communications program, ensuring quality execution and alignment with strategy.

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Track performance and apply insights to continuously improve communications effectiveness for the franchise.

Required Skills, Experience, and Education:

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10+ years of experience in biotech or pharmaceutical communications, including pipeline and product communications experience.Bachelor’s degree required in Communications or similar; advanced degree preferred.

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Demonstrated success supporting clinical development, regulatory milestones, and product launches, ideally in precision oncology or a similarly complex therapeutic area.

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Strong leadership presence with the ability to influence senior stakeholders and lead cross-functional initiatives.

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Deep understanding of the U.S. healthcare environment, including regulatory policy, R&D, pricing, and access.

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Exceptional storytelling and writing skills, with the ability to translate complex science for diverse audiences.

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Demonstrated experience managing sensitive issues and high profile communications.

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Track record of building relationships with top-tier scientific, medical, and industry media.

Preferred Skills:

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Deep familiarity with precision oncology, including competitive landscapes, combination strategies, and evolving standards of care.

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Proven success leading communications for major regulatory milestones, including FDA approvals, advisory committee meetings, and high-stakes data readouts.

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Strong issues-management experience relating to global trial

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