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
- Professional 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 in Toronto employer: Biopharma Careers
At Lilly Canada, we pride ourselves on fostering a collaborative and innovative work culture that empowers our Medical Science Liaison team to make a meaningful impact in the fields of Immunology, Gastroenterology, and Rheumatology. Our commitment to employee growth is evident through continuous learning opportunities, competitive compensation packages, and comprehensive benefits, including participation in the Lilly Bonus Program and flexible healthcare options. Located in Western Canada, our team enjoys a supportive environment that values scientific exchange and encourages building strong relationships with the medical community.
