ROLE RESPONSIBILITIES

• 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.

• Train and develop expertise in industry leading tool/skill for content creation. Ensure knowledge transfer with the broader MCCS team

 

Basic Qualifications

·       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 (eg, WORD, PowerPoint, Excel)

Preferred Qualifications

·       Experience in creating and developing medical content

·       Expertise in assigned therapeutic areas

·       ISMPP-CMPP®

·       Multimedia and omnichannel experience

·       Rapid adoption of new digital content, technology, and resources

·       Prior global exposure in professional/education settings

 
 

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical