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Johnson & Johnson is seeking a Director of Medical Writing to lead strategic discussions and oversee medical writing projects across various therapeutic areas. The ideal candidate will possess extensive experience in pharmaceutical writing and project management, with a strong emphasis on collaboration and communication.
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Job Summary
The Director of Regulatory Medical Writing is a recognized 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.
This role involves overseeing projects, identifying and mitigating risks, implementing process improvements, and guiding lead medical writers on compounds, contributing to TA-level strategies and organizational initiatives.
Responsibilities include acting as the primary interface for submission preparation, bringing scientific and regulatory submissions expertise to marketing applications, and leading early strategic submission discussions focusing on clinical scientific content.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking a Director of Medical Writing to lead strategic discussions and oversee medical writing projects across various therapeutic areas. The ideal candidate will possess extensive experience in pharmaceutical writing and project management, with a strong emphasis on collaboration and communication.
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Skills & Requirements
Must-have
extensive medical writing expertise
cross-functional team leadership
regulatory guidelines adherence
strategic submission discussions
process improvement implementation
Nice-to-have
inclusive work environment
respect diversity and dignity
championing patients
fosters organizational learning
Key Requirements
14+ years pharmaceutical/scientific experience
12+ years clinical/medical writing experience
University/college degree in scientific discipline