The Director of Regulatory Medical Writing is a leader with extensive medical writing expertise, serving as a primary liaison with cross-functional teams and driving strategic discussions
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 driving strategic discussions.
This role involves developing internal medical writers, ensuring adherence to best practices and regulatory guidelines, and overseeing projects with decision-making authority.
Responsibilities include influencing TA-level strategies, leading process working groups, championing internal standards, and improving internal systems and tools.
Matching 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 driving strategic discussions.
Skills & Requirements
Must-have
strategic medical writing leadership
people management experience
cross-functional team collaboration
regulatory guidelines adherence
process improvement implementation
Nice-to-have
inclusive work environment
championing patients
organizational learning
innovative medicine development
Key Requirements
University/college degree in scientific discipline
Minimum 14 years pharmaceutical/scientific experience
Minimum 12 years clinical/medical writing experience
Minimum 5 years people management experience
Expertise in project management and process improvement