Senior Manager, Medical Publications at Arrowhead Pharmaceuticals in Pasadena, CA
- Company: Arrowhead Pharmaceuticals
- Location: Pasadena, California, United States
- Salary: $150K – $175K
- Job type: full time
- Workplace: onsite
- Posted: 2026-10-14
All open roles at Arrowhead Pharmaceuticals
Job description
Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Senior Manager, Medical Publications will play a key role in developing high-quality, scientifically accurate, and strategically aligned medical publications deliverables that support Arrowhead’s Medical Affairs objectives. This individual will partner closely with internal cross-functional colleagues, external authors, and vendors to translate complex scientific and clinical data into clear, compliant, and impactful materials. This role will initially support the cardiometabolic program and may evolve to support additional pipeline programs across Arrowhead. This role is based in Pasadena with an expectation to be in office 5 days a week. Responsibilities Develop, write, edit, and coordinate high-quality medical publication deliverables, including abstracts, posters, oral presentations, manuscripts, slide decks, scientific narratives, lexicons, FAQs, and field medical resources Support the development and execution of integrated publication and congress plans, including identification of publication gaps, prioritization of analyses, journal/congress recommendations, and data dissemination opportunities. Translate complex clinical, scientific, and statistical information into clear, accurate, and compelling content for internal and external audiences Partner with cross-functional colleagues in Medical Affairs, Clinical Development, Biostatistics, Regulatory, Legal, Compliance, Medical Information, and Program Leadership to obtain input, resolve comments, and drive documents through review and approval processes Collaborate with internal and external authors in accordance with GPP and ICMJE criteria and company publication policies, supporting author engagement, document development, review cycles, and congress or journal submissions Maintain publication records, timelines, documentation, and compliance within publication management platforms and document review systems. Coordinate congress abstracts and journal manuscript submissions, including adherence to submission requirements, disclosures, copyright forms, and publication policies. Support publication advisory committee activities, authorship planning, journal selection, and scientific dissemination discussions in accordance with company publication policy and GPP. Manage timelines, review meetings, document versions, and stakeholder feedback to ensure writing deliverables are completed accuratel
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