Shape the future of cancer treatments with Johnson & Johnson as a Medical Writer II in Oncology. This hybrid role focuses on regulatory writing and supporting innovative medicine initiatives.

As a Medical Writer II within the Regulatory Medical Writing team, you will craft essential documents for Oncology projects. The position is pivotal for enhancing patient outcomes through detailed clinical documentation. You’ll engage in team collaborations and frequently interact with cross-functional members in various Therapeutic Areas while honing your writing expertise.

Key Responsibilities:



• Write clinical documents like Phase 1 protocols and CSRs • Coordinate and contribute to regulatory documents under supervision • Perform document quality control and literature reviews • Participate in cross-functional meetings and planning sessions • Track project milestones and timelines actively

Requirements: • Advanced scientific degree preferred; Bachelor's required • 2-4 years of regulatory medical writing experience • Robust written and oral communication skills • Ability to interpret scientific data effectively • Proven attention to detail and time management skills

Utilize your writing skills and scientific knowledge to advance Oncology research at Johnson & Johnson. #J-18808-Ljbffr

📌 Oncology Medical Writer II at Johnson & Johnson (Winnipeg)
🏢 Johnson & Johnson Innovative Medicine
📍 Winnipeg