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Responsibilities
- Independently author complex documents compliant with internal and regulatory standards
- Manage all aspects of document development and lead project teams
- Collaborate with teams to ensure effective presentation of analyses
- Develop project timelines and deliver documents on time
- Communicate document resource and timeline needs to project teams
- Identify and suggest process improvements to line management
- Serve as point of contact for document issues if assigned
- Produce documents with vendors as needed
Requirements
- Bachelor’s degree, preferably in life sciences
- BS/BA +7 years, MS/MA +5 years, PhD +2 years in medical writing
- Understanding of cross-functional team roles
- Ability to manage complex documents and multi-task
- Proficiency in MS Word, Excel, PowerPoint, Adobe
- Knowledge of Pfizer Global Style Guide and SOPs
- High fluency in English, strong oral presentation skills
- Experience with info graphics and regulatory guidance
- Ability to mentor junior colleagues
Benefits
- Annual base salary: $99,900.00 to $166,500.00
- Eligible for Pfizer’s Global Performance Plan (15% bonus target)
- Share-based long-term incentive program
- Comprehensive benefits: 401(k), paid leave, health coverage
- Potential relocation assistance
- Some travel (~5%) and global teleconference calls
