Johnson & Johnson is seeking a Manager, Regulatory Medical Writing to support across multiple therapeutic areas within IDAR. The role may be based in High Wycombe, UK, Leiden, NL, Neuss, DE, Paris, FR, Beerse, BE, or Horsham/Spring House/Raritan, US.
It is a Hybrid role (3 days onsite weekly) with potential remote options on case-by-case basis. The candidate will lead clinical document preparation, drive content strategy, and mentor junior writers while ensuring compliance with ICH guidelines
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