Pfizer

Manager - Medical Communications and Content Solutions (MCCS), Oncology

Posted 2 Days Ago

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Hiring Remotely in Maharashtra, IND

Remote

Mid level

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Develops and executes global medical content (manuscripts, abstracts, posters, slide decks, multimedia, plain-language summaries, systematic reviews) for assigned therapeutic areas. Collaborates cross-functionally, ensures data accuracy and compliance, manages project timelines, supports training and adoption of tools (including generative AI), and tracks project progress with guidance from team leads.

Summary Generated by Built In

Use Your Power for Purpose
By connecting evidence-based medical decision support with colleagues and stakeholders, you will help achieve better health and treatment outcomes. Your work will ensure our evidence is scientifically robust, provide unbiased and medically necessary expertise, and investigate ways to close data gaps. Your role is crucial in enabling the safe and appropriate use of medicines for patients, ultimately contributing to our mission of empowering healthcare decisions.
Role Summary
The Manager, Medical Communications and Content Solutions, Category Team within the Global Medical Communications and Content Solutions (MCCS) team in the Global & 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.
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 inassigned therapeutic areas
ISMPP-CMPP®
Multimedia and omnichannel experience
Rapid adoption of new digital content, technology, and resources
Prior global exposure in professional/education settings

Work Location Assignment: Remote
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

Skills Required

Advanced scientific doctoral degree (PhD, PharmD, MBBS/MD, MSc, MPH, MPharm)
Excellent scientific writing skills; ability to interpret and summarize complex data
Minimum of 3 years experience writing/developing medical content for pharmaceutical industry, academic settings, CRO, or biotech
Ability to lead and execute projects end-to-end
Strong interpersonal skills to build rapport with authors and external stakeholders across regions
Strong organizational skills; ability to prioritize multiple projects and meet deadlines with attention to detail
Understanding of statistical principles used in medical research and familiarity with epidemiologic principles
Effective English verbal and written communication
Demonstrated ability to lead projects independently and engage diverse stakeholders
Familiarity with software commonly used to present and analyze data (Word, PowerPoint, Excel)
Experience in creating and developing medical content
Expertise in assigned therapeutic areas (e.g., Oncology)
ISMPP-CMPP®
Multimedia and omnichannel experience; rapid adoption of new digital content and technology
Prior global exposure in professional/educational settings

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.