Medical Writing Manager

Pfizer

. Lead or co-lead moderately complex projects, managing time and resources .

Posted 10/5/2026full-timeRemote • United Kingdom, CanadaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in document quality control and medical writing within the pharmaceutical or biotech industry, with strong skills in project leadership, problem-solving, and effective communication. Proficient in utilizing AI tools to enhance productivity and ensure compliance with quality standards.

Highest-signal resume keywords

Document Quality ControlMedical WritingProject LeadershipAI Tools UtilizationInterpersonal Communication

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Document QCMedical WritingProject ManagementClinical TerminologyData PresentationQuality Control ReviewsTraining ColleaguesProblem-SolvingTime ManagementTask Prioritization

Soft Skills

Interpersonal SkillsCommunication SkillsCuriosityCollaborationMentoring

Tools & Technologies

Microsoft OfficeAI ToolsGenerative TechnologiesData Analysis Software

Industry Keywords

Pharmaceutical IndustryBiotech IndustryClinical TrialsRegulatory DocumentsQuality Standards

About the role

Key responsibilities & impact

Lead or co-lead moderately complex projects, 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 own work, seek feedback, and mentor colleagues by reviewing their work
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
Contribute to colleague training on quality standards and processes

Requirements

What you’ll need

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 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
Master's degree is highly desirable
Proficiency in software commonly utilized for data presentation and analysis
Strong problem-solving skills and ability to operate independently in ambiguous situations
Experience leading or co-leading projects
Experience 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
Curiosity for exploring how AI tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

Benefits

Comp & perks

Flexible workplace culture
Work-life harmony
Reasonable adjustments to support applications and future careers
Employee training and development opportunities