Johnson & Johnson is seeking a Director of Medical Writing, responsible for leading regulatory medical writing efforts across various therapeutic areas while ensuring adherence to industry standards. The ideal candidate will possess extensive experience in pharmaceutical writing, project management, and strategic decision-making in a collaborative environment
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 and ensuring adherence to best practices and regulatory guidelines.
Responsibilities include overseeing projects, identifying risks, implementing process improvements, guiding lead medical writers, and influencing TA-level strategies.
The role requires developing, implementing, and driving departmental process improvements and best practices, as well as mentoring and coaching staff.
Matching Summary
Match Score: 85
Johnson & Johnson is seeking a Director of Medical Writing, responsible for leading regulatory medical writing efforts across various therapeutic areas while ensuring adherence to industry standards. The ideal candidate will possess extensive experience in pharmaceutical writing, project management, and strategic decision-making in a collaborative environment.
Skills & Requirements
Must-have
medical writing expertise
cross-functional team leadership
regulatory guidelines adherence
strategic submission planning
process improvement implementation
Nice-to-have
inclusive work environment
mentoring and coaching staff
knowledge of industry trends
championing internal standards
Key Requirements
14 years of pharmaceutical/scientific experience
12 years of clinical/medical writing experience
Expertise in project management
Expertise in process improvement
University/college degree in a scientific discipline