Director, Scientific Publications

AstraZeneca•Boston, MA

4d•Hybrid

About The Position

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.

Requirements

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 required.
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) required.
Solid understanding of publication management databases (iEnvision, Datavision).

Nice To Haves

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.

Responsibilities

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.