Manager, Medical Communications and Content Solutions, Vaccines

About this role

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Skills you'll use

What you'll do

• The Manager will develop all relevant medical affairs content, including abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, multi-media and other types of external-facing medical content.
• Development of drafts includes researching, organizing, compiling, interpreting and quality check of various types of technical and/or medical information for straightforward projects with internal review support.
• Collaborate with the support of a more experienced colleague with cross-functional partners including medical communications & content teams, scientific publication committee teams, congress working teams, digital channel content teams and generative AI working groups to develop medical content across assigned therapeutic areas/medicines.
• With the support of a more experienced colleague, provide solutions to authors for assigned projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, Gen AI, etc.).
• Responsible for accuracy review and data quality control of all medical content to ensure that data is objectively and accurately represented.
• Ensure delivery of all projects within expected timelines while adhering to all quality and compliance requirements for medical content.
• Support more experienced colleagues in the development of training materials for product/therapeutic area priorities.
• Ensure training on relevant tools and processes, including new generative AI technology platforms, that ensure efficient and compliant execution of all medical affairs content.
• Track the progress of all assigned projects and resolve any issues/problems with guidance from the Team Lead.
• Stay abreast of evolving trends with medical content generation to ensure industry best practices are continuously leveraged.

Who can apply

• · Advanced scientific doctoral degree, (eg, PhD, PharmD, MBBS/MD, MSc, MPH, MPharm)
• Excellent scientific writing skills, including an ability to interpret and summarize complicated data effectively, concisely, and persuasively.
• Minimum of 3 years of experience in writing/developing medical content for the pharmaceutical industry, academic settings, CRO, or biotech company
• · Ability to lead and execute a project end-to-end
• · Strong interpersonal skills to quickly build rapport and credibility with authors and key external stakeholders cross culturally/regionally to drive solutions ahead.
• Strong organizational skills and ability to prioritize multiple projects and meet deadlines with strong attention to detail and follow-up with collaborators on a regular basis. Strong understanding of statistical principles used in medical research and familiarity with epidemiologic principles
• · Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings.
• · Demonstrated ability to lead projects independently and engage diverse stakeholders.
• · Understand the applications of technology to medical content development.
• · Experience with software commonly used to present and analyze data (e.g., Word, PowerPoint, Excel)

About Pfizer

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