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Director, Scientific Publications

AstraZeneca


Job Location:

Boston, MA - USA

Monthly Salary: Not provided by the employer
Posted: 29 September 2026 (6 days ago)
Application Deadline: 27 December 2026
Vacancies: 1 Vacancy

Job Summary

Job Title: Director Scientific Publications
Location: Boston MA

At AstraZeneca we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial thinking big and working together to make the impossible a reality. If you are swift to action confident to lead willing to collaborate and curious about what science can do then youre our kind of person.

Recognizing the importance of individualized flexibility our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office is purposely designed with collaboration in mind providing space where teams can come together to strategize brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people the planet and our business are interconnected which is why were taking ambitious action to tackle some of the biggest challenges of our time from climate change to access to healthcare and disease prevention.

Introduction to Role:
The Director Scientific Publications is 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 Plans 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. Effectively collaborates with key partners and ensures 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

  • Provides on-site support at key scientific congresses and meetings.

  • Ensures the high quality and transparency of publications by maintaining/promoting familiarity with ICMJE GPP3 CONSORT AMA and other external standards as well as AstraZeneca publication policies and procedures.

Essential Skills/Experience:

  • PhD PharmD MD or advanced scientific degree in a biomedical field with proven scientific and/or publications expertise

  • 5 years of experience in medical communications/publications in pharmaceutical/biotech industry medical communications agency CRO publishing or academic setting with equivalent work experience

  • Proven track record of collaborative 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)

  • Solid understanding of publication management databases (iEnvision Datavision)

Essential Skills/Experience:
  • 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

Total Rewards:

If in a Pay Transparent State

  • (Current: Maryland (Gaithersberg) California Colorado Hawaii New Jersey New York Washington Washington DC)
  • (Upcoming: Illinois & Minnesota (January 1 2025) Vermont (July 1 2025) Massachusetts (July 31 2025)
  • Virginiaas ofJuly 1 2026ANDMaineJuly 31st 2026

The annual base pay (or hourly rate of compensation) for this position ranges from $XXXXXX to $XXXXXX. Our positions offer eligibility for various incentivesan opportunity to receive short-term incentive bonuses equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs paid time off (i.e. vacation holiday and leaves) as well as health dental and vision coverage in accordance with the terms of the applicable plans.

Pay Transparency Verbiage:

The annual base pay (or hourly rate of compensation) for this position ranges from $XX to $XX TAqPartner will express compensation range as 80% - 120% of the roles MRP either asan annual base pay or as the hourly rate (annual salary divided by 2080 hours).Our positions offer eligibility for various incentivesan opportunity to receive short-term incentive bonuses equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs paid time off (i.e. vacation holiday and leaves) as well as health dental and vision coverage in accordance with the terms of the applicable plans.

If in Massachusetts (Waltham Boston)

As AstraZeneca continues to put patients at the forefront of our mission we are excited for our move to Kendall Square/Cambridge in 2026. Find out more information here: Kendall Square Press Release

AstraZenecais an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment assessment and selection process and may be requested by emailing.

#LI-Hybrid

Date Posted

14-Sept-2026

Closing Date

01-Oct-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and furtherance of that mission we welcome and consider applications from all qualified candidates regardless of their protected characteristics. If you have a disability or special need that requires accommodation please complete the corresponding section in the application form.


Required Experience:

Director


About Company

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AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more

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