Associate Director, Global Scientific Communications - Barcelona, España - Alexion Pharmaceuticals,Inc.

Alexion Pharmaceuticals,Inc.

Empresa verificada

Barcelona, España

hace 2 semanas

Publicado por:

Isabel García

beBee Recruiter

Descripción

Location:
Barcelona, Spain

Job reference:
R-192558

Date posted: 02/20/2024

Associate Director, Global Scientific Communications

Barcelona based, in office 3 days per week.

This is what you will do:

The Associate Director, Global Scientific Communications for centralized content creation (CCC) for META Plus is responsible for facilitating the successful development and execution of centralized content in alignment with global strategies.

The successful AD will collaborate closely with the Scientific Communication Indication leads, Medical Review leads, and Medical Directors, as well as the other internal stakeholders, to ensure adoption of centralized content and harmonization of medical communications across functions.

Developed materials should be market relevant and meet the needs of medical and commercial communications.

The CCC AD will manage the tactical development and maintenance of centralized content and the digital repository for centralized content.

The CCC AD will also work in coordination with the Operations Lead to drive efficiencies and enhancements and participate in the supervision of consultants and medical communication agencies.

You will be responsible for:

Developing, maintaining, and executing an annual materials plan in collaboration with the Sci Comms Leads, Global Medical Directors, and Medical Reviewers
Supporting the creation and update of Scientific Platforms
Leading the creation of Global Slide Libraries and other Sci Comms deliverables
Collaborating with internal stakeholders (e.g., US and international Medical Affairs, Research, Clinical Development, Commercial, Biostatistics Medical Information, Training, HEOR) to ensure that centralized content is aligned with global strategy
Collaborating with stakeholders and reviewers to resolve comments and escalate unresolved comments/issues through appropriate channels
Working closely with Medical review to ensure quality, review readiness, and approval for distribution
Leading communications plans to keep stakeholders informed
Overseeing operations for centralized content creation including organizing and leading relevant meetings, following up with action items
Ensuring that CCC material is updated, findable, and accessible
Working crossfunctionally with stakeholders to ensure other approved materials are up to date and accessible in the content repository
Serving as point person to answer questions regarding centralized content creation and leading trainings for internal stakeholders
Reporting on metrics that track centralized content use
Overseeing work of external consultants and agencies including budget and timelines
Coordinating with Operations Lead and Sci Comms excellence to ensure new processes are aligned crossTA and reflected in process documents
Contributing business knowledge to the assessment of system requirements for a centralized content digital platform

You will need to have:

Advanced degree: PhD, PharmD, or MD
35 years of relevant experience in a Pharmaceutical company
Strong project management skills
Experience in strategic content creation (eg scientific platforms and global slide libraries) and medical communications
Experience with Medical/Legal/Regulatory Review and Veeva platforms
Ability to interpret and organize highly complex scientific data
Ability to check accuracy of scientific data and statements against literature
Must be comfortable engaging with various types of digital platforms and programs such as Veeva, Docuvera, SharePoint, Smartsheet, Excel etc
Must be comfortable tracking and summarizing metrics data
Must have demonstrated ability to work independently
No travel is required

We would prefer for you to have:

Background or prior experience in META Plus
Demonstrated ability to write up/ review / edit scientific data
Strong working knowledge of current good publication practices and guidelines

AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.