Immunology Medical Writing Lead

6010-Biosense Webster Inc. Legal Entity; Belgique; Hybrid; EUR 80,000 - 138,000; Full time

Job summary

Johnson & Johnson is seeking a Manager, Regulatory Medical Writing in Immunology to lead the writing strategy and deliver high-quality clinical documents. You will manage cross-functional teams, influence content direction, and drive timelines with strong scientific leadership.

The role emphasizes mentorship, process improvement, and collaboration across regulatory and medical writing functions in a global setting.

Qualifications

• At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required.
• 2 years of people management experience is preferred.
• Excellent oral and written communication skills are pivotal to engage in cross-functional discussions.
• Expert project/time management skills.
• Strong project/process leadership skills.
• Ability to recognize how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content.
• Able to resolve complex problems independently.

Responsibilities

• Prepare and finalize all types of clinical documents.
• Lead in a team environment.
• Work with a high level of independence and take a lead role on assigned projects with respect to content and scientific strategy, timing, scheduling, and tracking.
• Lead or set objectives for others on team projects and tasks, eg, lead process working groups.
• Guide or train cross-functional team members on processes and best practices.
• May lead project-level/submission/indication writing teams.
• Proactively provide recommendations for departmental process improvements.

Skills

Attention to detail

Excellent communication

Project management

Leadership

Cross-functional collaboration

Medical writing

Regulatory knowledge (ICH)

Education

University/college degree

Masters or PhD preferred

Job description

Johnson & Johnson is seeking a Manager, Regulatory Medical Writing in Immunology to lead the writing strategy and deliver high-quality clinical documents. You will manage cross-functional teams, influence content direction, and drive timelines with strong scientific leadership.

The role emphasizes mentorship, process improvement, and collaboration across regulatory and medical writing functions in a global setting.