Medical Writing Lead: Flexible, Impactful Regulatory Docs

EasyInfoBlog.com LLC; United Kingdom; Remote; GBP 70,000 - 95,000; Full time

Benefits offered by this job

Flexible workplace culture

Disability adjustments

EOE and inclusive workplace commitment

Job summary

Pfizer in United Kingdom seeks a Medical Writing Manager to lead complex document projects, ensuring high-quality regulatory submissions and collaboration across multifunctional teams. The role emphasizes accuracy, adherence to standards, and mentoring colleagues in quality processes.

Requirements include advanced degrees and extensive experience in medical writing within pharma, with strong knowledge of clinical trials and terminology, plus proficiency in AI-enabled problem solving.

Qualifications

• Experience in document QC and/or medical writing in pharma/biotech.
• Interacts with cross-functional study teams effectively.
• Strong knowledge of medical terminology and clinical trials.
• Proficient in data presentation and reporting tools.

Responsibilities

• Lead or co-lead moderately complex projects with time/resource management.
• Develop document strategies and messages with project teams.
• Ensure documents meet internal standards and are submission-ready.
• Verify document accuracy using source materials including regulatory data.
• Lead authors for complex projects and perform QC reviews.
• Contribute to colleague training on quality standards and processes.

Skills

Project management

Cross-functional collaboration

Regulatory writing

Clinical terminology

Quality control

AI tools use

Education

Bachelor’s degree in life sciences

Master’s degree desirable

PhD/JD with relevant experience

Tools

MS Office

Data presentation tools

Job description

Pfizer in United Kingdom seeks a Medical Writing Manager to lead complex document projects, ensuring high-quality regulatory submissions and collaboration across multifunctional teams. The role emphasizes accuracy, adherence to standards, and mentoring colleagues in quality processes.

Requirements include advanced degrees and extensive experience in medical writing within pharma, with strong knowledge of clinical trials and terminology, plus proficiency in AI-enabled problem solving.