Manager, Medical Communications and Content Solutions

<p><span><b> ROLE SUMMARY</b></span></p><p><span>The Manager, Medical Communications and Content Solutions, Category Team within the Global Medical Communications and Content Solutions (MCCS) team in the Global &amp; US Medical Communications and Content (MCC) Organization is responsible for creating and executing global medical content end-to-end within a specific therapeutic area (Internal Medicine/ Specialty Care/ Vaccines/ Oncology), 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.</span></p><p><span><b>ROLE RESPONSIBILITIES</b></span></p><ul><li><p><span>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.</span></p></li><li><p><span>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.</span></p></li></ul><p><span>·       Collaborate with the support of a more experienced colleague with cross-functional partners including medical communications &amp; 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.</span></p><p><span> </span></p><ul><li><p><span>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.).</span></p></li></ul><p><span>·       Responsible for accuracy review and data quality control of all medical content to ensure that data is objectively and accurately represented.</span></p><ul><li><p><span>Ensure delivery of all projects within expected timelines while adhering to all quality and compliance requirements for medical content.</span></p></li><li><p><span>Support more experienced colleagues in the development of training materials for product/therapeutic area priorities.</span></p></li><li><p><span>Ensure training on relevant tools and processes, including new generative AI technology platforms, that ensure efficient and compliant execution of all medical affairs content.</span></p></li><li><p><span>Track the progress of all assigned projects and resolve any issues/problems with guidance from the Team Lead.</span></p></li><li><p><span>Stay abreast of evolving trends with medical content generation to ensure industry best practices are continuously leveraged.</span></p></li><li><p><span>Train and develop expertise in industry leading tool/skill for content creation. Ensure knowledge transfer with the broader MCCS team</span></p></li></ul><p><span> </span></p><p><span><b>Basic Qualifications</b></span></p><p><span style="color:#000000"><span>·       </span></span><span>Advanced scientific doctoral degree, (eg, PhD, PharmD, MBBS/MD, MSc, MPH, MPharm)</span></p><p><span style="color:#000000"><span>·       </span></span><span>Excellent scientific writing skills, including an ability to interpret and summarize complicated data effectively, concisely, and persuasively.</span></p><p><span style="color:#000000"><span>·       </span></span><span>Minimum of 3 years of experience in writing/developing medical content for the pharmaceutical industry, academic settings, CRO, or biotech company</span></p><p><span style="color:#000000"><span>·       </span></span><span>Ability to lead and execute a project end-to-end</span></p><p><span style="color:#000000"><span>·       </span></span><span>Strong interpersonal skills to quickly build rapport and credibility with authors and key external stakeholders cross culturally/regionally to drive solutions ahead.</span></p><p><span>·       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</span></p><p><span style="color:#000000"><span>·       </span></span><span>Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings.</span></p><p><span style="color:#000000"><span>·       </span></span><span>Demonstrated ability to lead projects independently and engage diverse stakeholders.</span></p><p><span style="color:#000000"><span>·       </span></span><span>Understand the applications of technology to medical content development.</span></p><p><span>Experience with software commonly used to present and analyze data (eg, WORD, PowerPoint, Excel)</span></p><p><span><b>Preferred Qualifications</b></span></p><p><span style="color:#000000"><span>·       </span></span><span>Experience in creating and developing medical content</span></p><p><span style="color:#000000"><span>·       </span></span><span>Expertise in assigned therapeutic areas</span></p><p><span style="color:#000000"><span>·       </span></span><span>ISMPP-CMPP®</span></p><p><span style="color:#000000"><span>·       </span></span><span>Multimedia and omnichannel experience</span></p><p><span style="color:#000000"><span>·       </span></span><span>Rapid adoption of new digital content, technology, and resources</span></p><p><span style="color:#000000"><span>·       </span></span><span>Prior global exposure in professional/education settings</span></p><p><span><b> </b></span></p><p><span><b>PHYSICAL/MENTAL REQUIREMENTS</b></span></p><p><span>N/A</span></p><p><span><b> </b></span></p><p><span><b>NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</b></span></p><p><span style="color:#000000"><span>·       </span></span><span>Travel up to 20-25%</span></p><p><span><b> </b></span></p><p><span> </span></p><p><span><b> </b></span></p><p><span><b>OTHER INFORMATION</b></span></p><p><span>N/A</span></p><p></p>&nbsp;<br>&nbsp;<br><p style="text-align:inherit"></p><p style="text-align:left"><span><span><span><span><span><span><span><span><span>Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</span></span></span></span></span></span></span></span></span></p><p style="text-align:inherit"></p><p style="text-align:inherit"></p>Medical<p></p><p></p>