Lead Medical Writer – Regulatory Oncology

Johnson & Johnson Innovative Medicine; Beerse; Hybrid; EUR 73,000 - 115,000; Full time

Benefits offered by this job

Hybrid work model

Competitive benefits

Job summary

Johnson & Johnson Innovative Medicine is seeking a Medical Writer III to support Oncology within our Integrated Data Analytics & Reporting (IDAR) team. The position offers hybrid onsite at Beerse, Belgium, with some remote options on a case-by-case basis.

You will write or coordinate clinical and regulatory documents and lead document planning with cross-functional teams. The role requires a science degree, 6+ years in pharma, including 4+ years in regulatory medical writing, and strong English

Qualifications

• University or college degree in a scientific field is required.
• At least 6 years of relevant pharmaceutical/scientific industry experience including 4 years regulatory medical writing.
• Oncology experience is preferred; ability to summarize complex data clearly.

Responsibilities

• Write or coordinate clinical and regulatory documents (CSRs, IBs, protocols, summaries, RMPs, responses).
• Lead cross functional document planning and review meetings with clinical teams.
• Mentor junior writers and manage timelines and project tracking.

Skills

Regulatory medical writing

Leadership

Team collaboration

Education

Bachelor's degree in a scientific discipline

Advanced degree (MS/PhD/MD) preferred

Job description

Johnson & Johnson Innovative Medicine is seeking a Medical Writer III to support Oncology within our Integrated Data Analytics & Reporting (IDAR) team. The position offers hybrid onsite at Beerse, Belgium, with some remote options on a case-by-case basis.

You will write or coordinate clinical and regulatory documents and lead document planning with cross-functional teams. The role requires a science degree, 6+ years in pharma, including 4+ years in regulatory medical writing, and strong English