Join Johnson & Johnson as a Regulatory Medical Writer II and contribute to groundbreaking Oncology research. This hybrid prospect emphasizes regulatory documentation and collaborative teamwork. In this role, you will support the Oncology therapeutic area by authoring key regulatory documents.

This position enables you to deepen your medical writing skills while working closely with cross-functional teams. Your contributions will play a crucial role in the development of life-changing treatments for patients. Key Responsibilities:

- Write and coordinate basic clinical documents and study protocols
- Develop and review low to medium complexity regulatory documents
- Execute document quality checks and perform literature searches
- Lead meetings for document planning and reviews
- Manage project timelines and dependencies effectively Requirements:
- Minimum Bachelor’s degree in a scientific field
- 2+ years of pharmaceutical or scientific experience
- Proficient written and verbal English communication
- Solid understanding of regulatory guidelines
- Ability to foster positive team relationships Enhance your medical writing career by impacting patient health outcomes at Johnson & Johnson.

📌 Regulatory Medical Writer II for Oncology (Toronto)
🏢 Johnson u0026 Johnson Innovative Medicine
📍 Toronto