Medical Writer III, Regulatory Medical Writing, X-TA in High Wycombe

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.

About 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.

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 in 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.

You Will Be Responsible For:

• Writing or coordinating clinical and regulatory documents such as, but not limited to, 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 document content and acting as a champion of medical writing processes and best practices.
• Establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed.
• Functioning as a lead writer on most compounds under supervision.
• Being the primary point of contact for medical writing activities for the cross‑functional team.
• Coaching or mentoring of more junior staff on document planning, processes, and content.
• Providing peer review as needed.
• Active participation in or leading process working groups.
• Resolving complex problems under supervision.

Qualifications / Requirements:

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

Benefits:

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 as we value work‑life balance. We offer career development opportunities for those who want to grow and be part of our organisation.

All qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that 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.

Required Skills: Medical Writing, Process Leadership, Regulatory Writing

Preferred Skills: Business Writing, Clinical Research and Regulations, Clinical Trials Operations, Coaching, Collaborating, Communication, Copy Editing, Data Synthesis, Industry Analysis, Medical Affairs, Medical Communications, Problem Solving, Process Oriented, Proofreading, Quality Standards, Research Ethics, Standard Operating Procedure (SOP)