Regulatory Medical Writer II — Lead Clinical Documents (Hybrid)

Johnson & Johnson is seeking a Medical Writer II, Regulatory Medical Writing, across multiple countries with a Hybrid work model (3 days onsite weekly). You will author diverse regulatory documents across Oncology, Immunology, Neuroscience, and more, supporting the IDAR team in global regulatory submissions.

The role is located in or near High Wycombe, UK, with potential postings in Beerse, NL, Leiden, and Neuss.

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