Johnson & Johnson Innovative Medicine in the United Kingdom is seeking a Medical Writer III for Regulatory Medical Writing to support Oncology projects within IDAR. The role is hybrid (3 days onsite weekly) and involves coordinating regulatory documents across cross-functional teams, with global collaboration and supervision as needed.
Applicants should have a science degree (advanced degree preferred) and at least 4 years of regulatory medical writing experience.
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Senior Regulatory Medical Writer – Oncology in High Wycombe employer: Johnson & Johnson Innovative Medicine
At Johnson & Johnson Innovative Medicine, we pride ourselves on fostering a collaborative and inclusive work culture that empowers our employees to thrive. As a Regulatory Medical Writer II, you will benefit from our commitment to professional development, with ample opportunities for growth and learning in a dynamic environment. Located in the UK, our hybrid work model offers flexibility while allowing you to contribute to impactful projects that advance healthcare globally.
Contact Details:
Johnson & Johnson Innovative Medicine Recruitment Team
