Associate Director, Regulatory Medical Writing, Oncology
Johnson & Johnson
Allschwil, Switzerland
**
Regulatory medical writing
Oncology therapeutic area
Lead writing teams independently
**
Johnson & Johnson is seeking an Associate Director of Regulatory Medical Writing in Oncology. The role requires extensive experience in regulatory writing, project management, and team leadership within the pharmaceutical industry, offering a fully remote work option.
**
Job Summary
Able to function as a lead writer on any compound independently and lead in setting functional tactics/strategy.
Responsible for leading compound/submission/indication/disease area writing teams independently and guiding or training cross-functional team members on processes and best practices.
Supervises/manages and is accountable for direct reports, setting objectives, providing performance oversight, and ensuring adherence to established policies.
Matching Summary
Match Score: 75
**
Johnson & Johnson is seeking an Associate Director of Regulatory Medical Writing in Oncology. The role requires extensive experience in regulatory writing, project management, and team leadership within the pharmaceutical industry, offering a fully remote work option.
**
Skills & Requirements
Must-have
Regulatory Medical Writing
Oncology therapeutic area
Lead writing teams independently
Process improvement initiatives
Cross-functional collaboration
Nice-to-have
Inspiring a world where complex diseases are prevented
Championing patients every step of the way
Inclusive work environment
Act as change agent
Key Requirements
Bachelor's Degree required
10 years pharmaceutical/scientific experience
8 years clinical/regulatory medical writing experience