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

Posted 7 Hours 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
Lead development and execution of global medical content for oncology, including manuscripts, congress materials, slide decks, multimedia, and plain-language summaries. Ensure accuracy, data quality, compliance, and timely delivery while collaborating cross-functionally, supporting training, adopting new content technologies (including generative AI), and tracking project progress under team guidance.
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 with ability to interpret and summarize complex data
  • Minimum of 3 years experience writing/developing medical content for pharmaceutical industry, academia, 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, prioritization, attention to detail, and follow-up
  • Strong understanding of statistical and epidemiologic principles used in medical research
  • Effective English verbal and written communication
  • Demonstrated ability to lead projects independently and engage diverse stakeholders
  • Familiarity with software for presenting and analyzing data (Word, PowerPoint, Excel) and applications of technology to medical content development
  • Experience creating and developing medical content
  • Expertise in assigned therapeutic areas (e.g., oncology)
  • ISMPP-CMPP® certification
  • Multimedia and omnichannel content experience
  • Prior global exposure in professional/education settings

What the Team is Saying

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Pfizer

Pfizer Compensation & Benefits Highlights

  • Healthcare Strength Multiple U.S. medical plan options include telehealth, comprehensive mental‑health support, fertility/family‑building benefits, transgender‑inclusive coverage, and certain Pfizer medications at no cost. A Wellbeing Wallet and wellness resources broaden the health and wellbeing offering.
  • Retirement Support A 401(k) with company matching is paired with an additional Pfizer Retirement Savings Contribution, alongside company‑paid life and disability insurance. One‑on‑one financial planning support is provided through Fidelity.
  • Leave & Time Off Breadth Paid time off spans vacation, holidays, and personal days, with additional caregiver and medical leave. U.S. parental leave commonly includes 12 weeks paid with options for additional unpaid bonding time and a return‑to‑work transition.

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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.

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Typical time on-site: 2.5 days a week
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