Enhance your career with Johnson & Johnson as a Regulatory Medical Writer II in oncology. This role, based in Toronto, supports our mission in innovative healthcare with hybrid work flexibility.

As a Medical Writer II within our Regulatory Medical Writing team, you will engage directly with oncology projects, producing critical regulatory documents that ensure compliance and clarity in communication. You will collaborate with cross-functional teams while developing your skills in writing protocols and clinical study reports. This position offers mentorship opportunities and a pathway to develop your writing and regulatory expertise.

Key Responsibilities:



• Create clinical and regulatory documents across various stages • Lead cross-functional document planning meetings • Conduct literature searches and document quality checks • Establish timelines and maintain document strategies • Guide junior team members in best practices

Requirements: • Scientific degree, advanced degree preferred • 2+ years of relevant writing experience in pharmaceuticals • Excellent written and verbal communication skills • Solid attention to detail and organizational abilities • Understanding of medical and regulatory guidelines

Leverage your medical writing talent to make a significant impact on healthcare solutions at Johnson & Johnson. #J-18808-Ljbffr

📌 Regulatory Medical Writer II - Oncology (Winnipeg)
🏢 Biopharma Careers
📍 Winnipeg