Medical Writing Manager

Job not on LinkedIn

🔥 0 minutes ago

🌐 United Kingdom, Canada – Remote

🇬🇧 United Kingdom – Remote 🇨🇦 Canada – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✏️ Content Writer

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Pfizer

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1849

💼 Consulting

📣 Marketing

💊 Pharmaceuticals

💰 Post-IPO Debt on 2023-05

Consulting • Marketing • Pharmaceuticals

Pfizer is a pharmaceutical company that has been at the forefront of scientific innovation for 175 years. The company is dedicated to improving health and well-being at every stage of life by providing access to safe, effective, and affordable medicines and healthcare services. Pfizer focuses on delivering innovative therapies, particularly in the field of cancer treatments, as it continues to progress in transforming the healthcare landscape.

📋 Description

• Lead or co-lead moderately complex projects, managing time and resources • Apply skills and knowledge to contribute to departmental work • Resolve moderately complex problems and operate independently in ambiguous situations, guided by policies • Independently complete assignments, seeking 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

• 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 about improving outcomes with AI tools and understanding of responsible AI practices, including risk management and ethical use

🏖️ Benefits

• Flexible workplace culture supporting work-life harmony • Reasonable adjustments for applicants and employees with disabilities • Equal employment opportunity and inclusive workplace commitment