At a Glance
- Tasks: Lead the creation of clinical documents and mentor junior writers in a dynamic team.
- Company: Join Johnson & Johnson, a global leader in healthcare innovation.
- Benefits: Enjoy a hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Flexible remote options available; thrive in a supportive and innovative environment.
- Why this job: Make a real impact in healthcare by driving scientific strategy and collaboration.
- Qualifications: Experience in regulatory medical writing and strong leadership skills.
The predicted salary is between 63000 - 77000 £ per year.
Johnson & Johnson in High Wycombe, UK, is seeking a Manager, Regulatory Medical Writing to support across key therapeutic areas within Integrated Data Analytics & Reporting. This hybrid role (3 days onsite weekly) may be located in multiple countries; remote options may be considered case-by-case.
You will lead the preparation and finalization of clinical documents, drive content and scientific strategy, and mentor junior writers while coordinating with cross-functional teams to ensure.
Regulatory Medical Writing Manager — Lead Clinical Documents in High Wycombe employer: 7360-Janssen-Cilag Limited Legal Entity
At Johnson & Johnson, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work environment in High Wycombe, where innovation thrives. Our commitment to employee growth is evident through extensive training opportunities and a culture that values diversity and collaboration, empowering you to make a meaningful impact in healthcare. Join us to be part of a team that not only champions patients but also fosters your professional development and well-being.
Contact Details:
7360-Janssen-Cilag Limited Legal Entity Recruitment Team
