Responsibilities

• Own and lead the integrated pipeline and product communications strategy across all stages of development, ensuring clear differentiation, scientific credibility, and alignment with corporate and business priorities.
• Direct communications for major clinical and regulatory milestones, including data readouts, congress presentations, trial initiations, filings, approvals, and pre-launch milestones, in close partnership with R&D, Medical Affairs, Regulatory, and Legal.
• Serve as the senior communications advisor for launch readiness, shaping pre-launch and launch narratives across earned media, disease education, patient engagement, and stakeholder communications, with clear linkage to future commercial strategy.
• Lead disease awareness and patient advocacy communications, ensuring responsible education, strong patient advocacy group partnerships, and integration of patient voice into pipeline and product storytelling.
• Provide strategic counsel on value, access, and product-related issues, anticipating reputational risk and leading communications response to safety updates, competitive dynamics, and external scrutiny.
• Drive scientific and medical thought leadership, positioning Revolution Medicines and its leaders as credible voices through publications, congress presence, executive visibility, and media engagement.
• Build and lead a high-performing pipeline and product communications team, setting direction, developing talent, and ensuring consistent, high-quality execution.
• Oversee agency partners and measurement frameworks, using insights to evaluate impact, optimize performance, and scale communications effectiveness.

Requirements

• 15+ years of experience in biotech or pharmaceutical communications, including deep experience in pipeline and product communications in-house and/or at a leading agency.
• Bachelor’s degree required in Communications or similar; advanced degree preferred
• Demonstrated success supporting clinical development, regulatory milestones, and product launches, ideally in precision oncology or a similarly complex therapeutic area.
• Proven people management experience, including leading teams and developing talent.
• Strong leadership presence with the ability to influence senior stakeholders and lead cross-functional initiatives.
• Deep understanding of the U.S. healthcare environment, including regulatory policy, R&D, pricing, and access.
• Exceptional storytelling and writing skills, with the ability to translate complex science for diverse audiences.
• Demonstrated experience managing sensitive issues and high-profile communications.
• Track record of building relationships with top-tier scientific, medical, and industry media.

Preferred

• Deep familiarity with precision oncology, including competitive landscapes, combination strategies, and evolving standards of care.
• Proven success leading communications for major regulatory milestones, including FDA approvals, advisory committee meetings, and high-stakes data readouts.
• Strong issues-management experience relating to global trial access and expanded access.
• Track record of coordinating with corporate patient advocacy and patient advocacy organizations and integrating patient voice into pipeline and product storytelling.
• History of leading large-scale disease education or awareness campaigns that shift understanding of disease complexity or heterogeneity.
• Background spanning both product and corporate communications, enabling integrated decision-making across asset narratives and enterprise reputation.

Benefits

• strong benefits
• significant learning and development opportunities