Director, Pipeline & Product Communications

Key Responsibilities

• 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.
• Lead communications execution for clinical milestones, including data readouts, abstracts, presentations, and major medical congresses.
• 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.
• 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.
• Support regulatory and pre-launch communications, including trial initiations, regulatory submissions, approvals, and launch readiness activities.
• Execute disease awareness and patient advocacy communications in partnership with Patient Advocacy, ensuring responsible education and inclusion of patient voice.
• Support communications related to value, access, and product-specific issues, in coordination with Market Access, Legal, and Corporate Communications.
• Contribute to scientific and medical thought leadership efforts, including congress presence, publication support, speaker positioning, and external engagement.
• Manage agency partners and external vendors supporting the tumor-specific communications program, ensuring quality execution and alignment with strategy.
• Track performance and apply insights to continuously improve communications effectiveness for the franchise.

Required Skills, Experience, and Education

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