Logo for Pfizer

Medical Writing Manager

Role overview

Qualifications

  • BA/BS or MBA/MS with some relevant experience or PhD/JD with any relevant experience or Associate's degree with strong relevant experience or High School Diploma (or Equivalent) with extensive relevant experience
  • Demonstrated experience in document QC and/or medical writing in the pharmaceutical or biotech industry
  • Excellent interpersonal and communication skills
  • Proficiency with Microsoft Office applications

Responsibilities

  • Lead or co-lead moderately complex projects, effectively managing time and resources
  • Review your own work, seek feedback from others, and mentor colleagues by reviewing their work
  • Ensure documents meet internal standards, are submission-ready, and properly stored
  • Collaborate with project team experts to develop document strategies and messages

Key facts

Hard skills

Other skills

  • Communication
  • Social Skills
  • Mentorship
  • Microsoft Office
  • Problem Solving
  • Time Management
  • Prioritization

About the company

Pfizer logo

Pfizer

Pharmaceutical Manufacturing

We’re celebrating 175 years of daring scientific innovation—and we’re not done yet. Every day, we’re channeling our passion and resources into delivering innovative therapies that change the face of healthcare. Let’s outdo yesterday. Follow our progress as we accelerate the next generation of cancer treatments at LetsOutdoCancer.com For additional information on our guidelines, please visit http://www.pfizer.com/community-guidelines

Company details

IndustryPharmaceutical Manufacturing
Company size10001

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

Job description

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.

What You Will Achieve

In this role, you will:

  • Lead or co-lead moderately complex projects, effectively managing time and resources.
  • Apply skills and knowledge to contribute to departmental work.
  • Make decisions to resolve moderately complex problems and operate independently in ambiguous situations, guided by policies.
  • Work independently on assignments, receiving guidance on unusual or complex problems.
  • Review your own work, seek feedback from others, and mentor colleagues by reviewing their work.
  • Utilize judgment and experience to potentially become a resource for others.
  • Collaborate with project team experts to develop document strategies and messages.
  • Ensure documents meet internal standards, are submission-ready, and properly stored.
  • Verify document accuracy using source materials, including clinical regulatory documents and data.
  • Lead teams of authors for complex projects, perform Quality Control reviews, and contribute to colleague training on quality standards and processes.

Here Is What You Need (Minimum Requirements)


  • BA/BS or MBA/MS with some relevant experience or PhD/JD with any relevant experience or Associate's degree with strong relevant experience or High School Diploma (or Equivalent) with extensive relevant experience
  • Demonstrated experience in document QC and/or medical writing in the pharmaceutical or biotech industry
  • Experience in interacting with cross-functional study team members
  • Solid understanding of medical terminology and clinical trials
  • Excellent interpersonal and communication skills
  • Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives
  • Proficiency with Microsoft Office applications

Bonus Points If You Have (Preferred Requirements):


  • Master's degree is highly desirable
  • Proficiency in software commonly utilized for data presentation and analysis
  • Strong problem-solving skills and the ability to operate independently in ambiguous situations
  • Experience in leading or co-leading projects
  • Experience in training colleagues on quality standards and processes
  • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

  

Work Location Assignment: Remote within UK or Canada


Closing date for applications is October 19th 2026.

Purpose 

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.  

Digital Transformation Strategy

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Flexibility  

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!  

Equal Employment Opportunity 

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

DisAbility Confident

We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!

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

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Medical Scribe Related jobs

Other jobs at Pfizer

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.