Associate Director, Scientific Publications

14 hours ago

Cambridge, United Kingdom AstraZeneca Full time

The Associate 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 Associate Director will be responsible for the development of aspects of a Publication Plan, in collaboration with other team members and under the supervision of the Publications Director. The Associate Director will also have the opportunity to collaborate cross-functionally and ensure publication plans align with project strategy


**Typical Accountabilities**:

- Leads the publication development process to deliver high-quality publications, participating as a member of cross-functional teams, effectively collaborating with key partners, and ensuring compliance with internal and external publication guidelines.
- Collaborate cross-functionally to deliver 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.
- Provide 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 Qualifications
- PhD, PharmD, MD, or advanced scientific degree in a biomedical field with proven scientific and/or publications expertise strongly preferred. Non-terminal degree in biomedical discipline or equivalent with in depth experience in publication management considered
- 3-5 years of experience in medical communications/publications in pharmaceutical/biotech industry, medical communications agency, CRO, publishing or academic setting with equivalent work experience
- Demonstrated project management, organization, and time management skills
- Excellent oral and written communication skills and interpersonal skills
- Awareness of pharmaceutical publication practices such as GPP and ICMJE

**Skills**:

- Basic knowledge and understanding of publication strategy and planning
- Previous experience with management of contract resources/vendors
- Knowledge/Understanding of GPP3, ICMJE, AMA, and other publication standards
- Ability to analyze critically and synthesize scientific information from a broad range of scientific disciplines and clinical therapeutic areas
- Strong interpersonal, communication, and leadership skills
- Ability to work collaboratively with diverse teams

Desired Qualifications
- Previous experience in oncology
- Experience in working in Publication tracking software such as Datavision or PubStrat
- AMWA, BELS, and/or ISMPP (CMPP) certification

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