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
Janssen-Cilag Limited is an exceptional employer that fosters a collaborative and innovative work culture in High Wycombe, England. With a strong commitment to employee development, we offer extensive growth opportunities through mentorship and training, ensuring our team members thrive in their careers while contributing to impactful clinical programming strategies. Our focus on operational excellence and compliance not only enhances the quality of our work but also creates a rewarding environment for those passionate about advancing healthcare.
Contact Details:
7360-Janssen-Cilag Limited Legal Entity Recruitment Team
