At a Glance
- Tasks: Create impactful regulatory documents in various therapeutic areas like oncology and neuroscience.
- Company: Join the innovative team at Johnson & Johnson, a leader in healthcare.
- Benefits: Enjoy hybrid work options, competitive salary, and opportunities for professional growth.
- Other info: Work in a dynamic environment with a focus on innovation and teamwork.
- Why this job: Make a difference in healthcare by contributing to vital medical writing projects.
- Qualifications: Experience in regulatory medical writing and strong collaboration skills required.
The predicted salary is between 45000 - 55000 £ per year.
Johnson & Johnson is seeking a Medical Writer II, Regulatory Medical Writing, to support multiple therapeutic areas within IDAR.
The role may be located in Beerse, Belgium; High Wycombe/Maidenhead, UK; or Neuss, Germany.
It is a hybrid role with three onsite days weekly and limited remote options considered case-by-case.
You will author diverse regulatory medical writing documents across oncology, immunology, neuroscience, and more, coordinating with cross-functional teams and contributing to
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Regulatory Medical Writer II — Hybrid/Remote Options employer: Johnson & Johnson
At Johnson & Johnson, we pride ourselves on being an exceptional employer, fostering a culture of inclusivity and respect for diversity. Our Leeds location offers employees the opportunity to work at the forefront of healthcare innovation, with access to comprehensive training and development programmes that support personal and professional growth. Join us to be part of a team that is dedicated to making a profound impact on health for humanity while enjoying a collaborative and supportive work environment.
