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Johnson & Johnson is seeking a Director of Medical Writing in High Wycombe, UK, to lead medical writing efforts across various therapeutic areas. The ideal candidate will have extensive experience in clinical and regulatory writing, project management, and the ability to mentor writing teams while ensuring adherence to best practices and regulatory guidelines.
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Job Summary
The Director of Regulatory Medical Writing is a leader with extensive medical writing expertise, serving as a primary liaison with cross-functional teams to drive strategic discussions and ensure adherence to best practices and regulatory guidelines.
Responsibilities include overseeing projects, identifying risks, implementing process improvements, guiding lead medical writers, influencing TA-level strategies, and leading process working groups.
The role requires scientific and regulatory submission expertise for marketing applications, acting as a subject matter expert for submission strategy and developing/maintaining submission training materials.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking a Director of Medical Writing in High Wycombe, UK, to lead medical writing efforts across various therapeutic areas. The ideal candidate will have extensive experience in clinical and regulatory writing, project management, and the ability to mentor writing teams while ensuring adherence to best practices and regulatory guidelines.
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Skills & Requirements
Must-have
medical writing expertise
cross-functional team leadership
regulatory guidelines adherence
strategic discussions
process improvement implementation
Nice-to-have
inclusive work environment
diversity and dignity
merit recognition
science-based advancements
patient-centric approach
Key Requirements
14 years of relevant pharmaceutical/scientific experience
12 years of relevant clinical/medical writing experience
University/college degree in scientific discipline