Apply regulatory medical writing expertise to oncology documents at Johnson & Johnson in a hybrid Toronto position with three onsite days weekly.

As Medical Writer III, you will support Oncology within Integrated Data Analytics & Reporting. You will independently handle documents within your therapeutic area and work under supervision across areas. The position involves clinical and regulatory writing, planning, review coordination, and process participation.

Key Responsibilities:

- Write or coordinate clinical and regulatory documents
- Lead cross-functional document planning and review meetings
- Establish document timelines and strategies
- Serve as medical writing contact for teams
- Coach junior staff and provide peer review

Requirements:

- University degree in a scientific discipline
- At least six years of relevant industry experience
- At least four years of regulatory medical writing experience
- Ability to interpret and present statistical medical information
- Qualified written and spoken English proficiency

Bring oncology knowledge, regulatory writing capability, and cross-functional leadership to Johnson & Johnson’s Toronto medical affairs team.

📌 Oncology Regulatory Medical Writer (Toronto)
🏢 Biopharma Careers
📍 Toronto