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Director, Scientific PublicationsAstraZeneca · US - Boston - MA
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AstraZeneca

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Director, Scientific Publications

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🗓️ Posted 2026-09-15 US - Boston - MA Full-time Hybrid Science Technology
💰 Salary Not shared 📊 Market 10,833 GBP–16,667 GBP/mo

About the Company

T he Director, Scientific Publications i s responsible for the development of high-quality clinical publications and reviews for investigational pipeline products in Oncology R& D. In addition, the Director will be responsible for the development and delivery of strategic Publication Plan s for pipeline assets. The Director will also have the opportunity to lead cross-functional publication teams, ensure publication plans align with project and overall Oncology R&D strategy, and ensure that these partnerships are successful and that plans represent a transparent and fair balanced communication of data. Accountabilities: Leads the cross-functional team responsible for the publication development process to deliver high-quality publication . E ffectively collaborat es with key partners and ensu res compliance with internal and external publication guidelines. Leads the cross-functional team to deliver strategic publications plans that are aligned with project strategy. Accountable for managing 3rd-party providers in the delivery of defined publications activity, ensuring quality and delivery standards are adhered to Develops and ensures that strategically aligned scientific communication points are delivered and that statements and conclusions in publications are accurate and supported by appropriate data . Uses subject matter expertise to provide publications insight to partners, collaborators, and more junior team members Pr

Requirements

  • ● PhD, PharmD, MD or advanced scientific degree in a biomedical field with proven scientific and/or publications expertise
  • ● + years of experience in medical communications/publications in pharmaceutical/biotech industry, medical communications agency, CRO, publishing, or academic setting with equivalent work experience required
  • ● Proven track record of c ollaborative and consultative cross-matrix abilities
  • ● The ability to appreciate and work within a large strategic framework, while maintaining strong attention to detail and compliance to global publications ethical standards and company publications policy and SOPs
  • ● Ability to understand and adhere to good publication practices and relevant guidelines on and scientific data communication, such as ICMJE, GPP3, company policy and SOPs
  • ● Detailed working knowledge and understanding of publication strategy and planning
  • ● Previous experience with management of contract resources/vendors
  • ● Demonstrated ability and flexibility to prioritize while supporting multiple projects, dealing effectively with change and ambiguity
  • ● Broad understanding of drug development process
  • ● Demonstrated ability to establish and maintain professional relationships with external experts, investigators, journal editors and publishers and professional bodies
  • ● Working knowledge of Datavision publication management systems
  • ● Demonstrated ability to mentor others during the flow of work
  • ● Proficiency in Microsoft Office applications (Word, Excel, Powerpoint ) required
  • ● Solid understanding of publication management databases ( iEnvision , Datavision)
  • ● AMWA, BELS, and/or ISMPP (CMPP) certification
  • ● Background in biologics and/or previous experience in oncology products
  • ● Previous experience writing and editing peer-reviewed clinical publications highly desirable
  • ● Where can I find out more
  • ● Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/
  • ● Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/