Pfizer
Associate Manager, Medical Communications and Content Solutions- Vaccines
Be an Early Applicant
Develop and quality-check global external-facing medical content (abstracts, manuscripts, posters, graphical abstracts, slide decks, multimedia, plain language summaries). Collaborate with stakeholders and cross-functional teams, ensure compliance and timelines, adopt new tools (including generative AI), and track project progress with manager oversight.
ROLE SUMMARY
The Associate Manager, Medical Communications and Content Solutions, within the Global Medical Communications and Content Solutions (MCCS) team in the Global & US Medical Communications and Content (MCC) Organization is responsible for , developing global medical 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 under supervision.
• The Associate Manager will develop with support and supervision, 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.
• Responsibilities may include researching, organizing, compiling, interpreting, and quality check of various types of technical and/or medical content.
• Provide solutions to stakeholders in alignment with manager for all projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, etc.).
• Ensure execution of all projects within expected timelines while adhering to all quality and compliance requirements for medical content.
• 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 projects and resolve any issues/problems with guidance from manager.
Basic Qualifications
• Advanced scientific degree, (eg, MS, MRes, MPharm, PhD, PharmD, MBBS/MD)
• 2+ years experience in pharmaceutical medicine, including medical affairs, medical compliance.
• Proven ability to take ownership of individual work and align with more experienced colleagues on scope, timelines, quality expectations, etc.
• Strong interpersonal skills to quickly build rapport and credibility with colleagues and key external stakeholders cross culturally/regionally.
• Experience in medical content writing /writing in academic settings/ communications experience within an agency, CRO, Pharma / Biotech Company.
• Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings
• Demonstrated ability to work effectively in a team and understand the applications of technology to medical content development
Preferred Qualifications
• Expertise in assigned therapeutic areas
• Experience in medical content creation
• Multimedia and omnichannel experience
• Rapid adoption of new digital content, technology, and resources
• Global / international work or educational experience
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical
The Associate Manager, Medical Communications and Content Solutions, within the Global Medical Communications and Content Solutions (MCCS) team in the Global & US Medical Communications and Content (MCC) Organization is responsible for , developing global medical 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 under supervision.
• The Associate Manager will develop with support and supervision, 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.
• Responsibilities may include researching, organizing, compiling, interpreting, and quality check of various types of technical and/or medical content.
• Provide solutions to stakeholders in alignment with manager for all projects and collaborate with other teams to drive these solutions (Graphics, Compliance agency, Statistics teams, etc.).
• Ensure execution of all projects within expected timelines while adhering to all quality and compliance requirements for medical content.
• 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 projects and resolve any issues/problems with guidance from manager.
- Identify and train to become an expert on one new tool/skill for content creation representing the latest trends in the industry.
Basic Qualifications
• Advanced scientific degree, (eg, MS, MRes, MPharm, PhD, PharmD, MBBS/MD)
• 2+ years experience in pharmaceutical medicine, including medical affairs, medical compliance.
• Proven ability to take ownership of individual work and align with more experienced colleagues on scope, timelines, quality expectations, etc.
• Strong interpersonal skills to quickly build rapport and credibility with colleagues and key external stakeholders cross culturally/regionally.
• Experience in medical content writing /writing in academic settings/ communications experience within an agency, CRO, Pharma / Biotech Company.
• Effective English verbal and written communication with flexibility to be clear, consistent, compliant, and appropriate for a variety of settings
• Demonstrated ability to work effectively in a team and understand the applications of technology to medical content development
Preferred Qualifications
• Expertise in assigned therapeutic areas
• Experience in medical content creation
• Multimedia and omnichannel experience
• Rapid adoption of new digital content, technology, and resources
• Global / international work or educational experience
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical
Similar Jobs at Pfizer
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Develop and quality-check global medical affairs content (manuscripts, abstracts, posters, slide decks, multimedia, plain-language summaries). Coordinate with stakeholders and cross-functional teams, ensure compliance and timelines, adopt new content tools including generative AI, and track project progress under manager supervision.
Top Skills:
Generative Ai
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Develop and quality-check global medical affairs content (manuscripts, abstracts, posters, slide decks, multimedia, plain-language summaries). Coordinate with stakeholders and cross-functional teams, ensure compliance and timelines, adopt new content tools including generative AI, and track project progress under manager supervision.
Top Skills:
Generative Ai
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Lead administration and continuous improvement of Veeva eQMS for Regulatory Quality Assurance. Own access management, release coordination, reporting, and user documentation. Provide Vault configuration expertise, triage enhancement requests, represent Digital Systems in cross-functional programs, support data extracts and reporting, and drive AI-enabled process improvements and platform transformation within a GxP-regulated pharmaceutical environment.
Top Skills:
Ai-Enabled ToolsDataikuDssEqmsMicrosoft Power AutomatePower BISnowflakeSpotfireSQLVeevaVeeva Vault Eqms
What you need to know about the Dublin Tech Scene
From Bono and Oscar Wilde to today's tech leaders, Dublin has always attracted trailblazers, with more than 70,000 people working in the city's expanding digital sector. Continuing its legacy of drawing pioneers, the city is advancing rapidly. Ireland is now ranked as one of the top tech clusters in the region and the number one destination for digital companies, with the highest hiring intention of any region across all sectors.
