Medical Writing Manager role at Pfizer supporting evidence-based medical decision-making and regulatory documentation. The position involves leading or co-leading moderately complex projects, ensuring document quality and accuracy, and collaborating with cross-functional teams to develop submission-ready materials.
Responsibilities
- Lead or co-lead moderately complex projects while managing time and resources effectively
- Review documents for accuracy, internal standards compliance, and submission readiness
- Collaborate with project teams to develop document strategies and messaging
- Lead author teams for complex projects and perform quality control reviews
- Mentor colleagues by reviewing their work and providing feedback on quality standards
Requirements
- Bachelor's degree or higher in relevant field; Associate's degree with strong experience; or High School Diploma with extensive experience
- Demonstrated experience in document quality control and/or medical writing in pharmaceutical or biotech
- Experience collaborating with cross-functional study teams
- Solid understanding of medical terminology and clinical trials
- Excellent interpersonal and communication skills
- Ability to manage multiple priorities and execute tasks within objectives
- Proficiency with Microsoft Office applications
Vacancy posted more than 2 months ago
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