Medical Writer III, Regulatory Medical Writing, X-TA

Medical Writer III, Regulatory Medical Writing, X-TA

Join to apply for the Medical Writer III, Regulatory Medical Writing, X-TA role at Johnson & Johnson Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science‑based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at

We are searching for the best talent for a Medical Writer III, Regulatory Medical Writing to support across key therapeutic areas (X-TA) within our Integrated Data Analytics & Reporting (IDAR) business. The position may be located High Wycombe, UK;
Leiden, Netherlands;
Neuss, Germany;
Paris, France; or Beerse, Belgium
. The position is Hybrid (3 days onsite weekly). Remote work options may be considered on a case‑by‑case basis and if approved by the company. This role is available across multiple countries; please apply to the posting that aligns with your preferred location.

• Writing or coordinating clinical and regulatory documents such as CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents.
• Leading cross‑functional document planning and review meetings, interacting with cross‑functional colleagues on content, and championing medical writing processes and best practices.
• Establishing document timelines and strategies in accordance with internal processes, with guidance from functional management and clinical team as needed.
• Acting as lead writer on most compounds (or submissions, indications, or disease areas) under supervision and primary point of contact for medical writing activities for the cross‑functional team.
• Coaching or mentoring junior staff on document planning, processes, and content, and providing peer review as needed.
• Actively participating in or leading process working groups.

• A university/college degree in a scientific discipline is required; an advanced degree (Masters, PhD, MD) preferred.
• At least 6 years of relevant pharmaceutical/scientific experience; at least 4 years of relevant medical writing experience.
• Excellent oral and written communication skills to engage in cross‑functional discussions.
• English fluency required.
• Attention to detail.
• Ability to function in a team environment.
• Strong project and time‑management skills.
• Strong project/process leadership skills.
• Ability to resolve complex problems under supervision.
• Demonstrated learning agility.
• Ability to build solid and productive relationships with cross‑functional team members.

We offer a competitive salary and extensive benefits package. The health and well‑being of our employees is a priority; we have a flexible working environment and value work‑life balance. We offer career development opportunities. For additional general information on company benefits, please go to:

All qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodations.