The Director of Regulatory Medical Writing is a recognized leader with extensive medical writing expertise across various therapeutic areas, serving as a primary liaison with cross-functional teams
Job Summary
The Director of Regulatory Medical Writing is a recognized leader with extensive medical writing expertise across various therapeutic areas, serving as a primary liaison with cross-functional teams.
This role involves overseeing projects, identifying risks, implementing process improvements, and guiding lead medical writers on compounds with the same or different indications.
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 recognized leader with extensive medical writing expertise across various therapeutic areas, serving as a primary liaison with cross-functional teams.
Skills & Requirements
Must-have
extensive medical writing expertise
cross-functional team leadership
regulatory guidelines adherence
strategic submission planning
process improvement implementation
Nice-to-have
inclusive work environment
patient-centric approach
innovative medicine development
mentoring and coaching staff
industry standards representation
Key Requirements
University/college degree in a scientific discipline
Minimum 14 years of pharmaceutical/scientific experience
Minimum 12 years of clinical/medical writing experience