Regulatory Medical Writer II — Lead Clinical Documents; Hybrid
Listed on 2026-10-11
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Healthcare
Medical Science Liaison, Medical Science
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.
Step into the Regulatory Medical Writer II — Lead Clinical Documents (Hybrid) role at Johnson Johnson in High Wycombe, England, United Kingdom and grow with us.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Regulatory Medical Writer II — Lead Clinical Documents (Hybrid) role in the description above.
We appreciate your interest in this position.
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