Medical Writer III, X-TA

Johnson & Johnson is hiring a Medical Writer III, X-TA. Level rates it ; you can apply on Johnson & Johnson.

Level's read on this job

Level rates this role Little AI ●○○○: aI is not part of the work.
The posting mentions medical writing, regulatory writing and clinical data among its tools and skills.
Level classes it as a senior role.
Johnson & Johnson has 1,900+ other open roles on Level.
Posted within the past two weeks.

AI in this role

Medical Writer III responsible for regulatory medical writing and documentation across key therapeutic areas.

medical-writingregulatory-writingclinical-data

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. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Medical Affairs Group

Job Sub Function:

Medical Writing

Job Category:

Professional

All Job Posting Locations:

High Wycombe, Buckinghamshire, United Kingdom

Job Description:

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.

Learn more at https://www.jnj.com/innovative-medicine

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 Maidenhead, 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.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

United Kingdom -Requisition Number: R-103733
Belgium/Netherlands/France/Germany - Requisition Number: R-104917

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Are you ready to join our team? Then please read further!

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 (eg, with clinical team) 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. Responsible for establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed.
Will function as a lead writer on most compounds (or submissions, indications, or disease areas) under supervision. Will be primary point of contact for medical writing activities for the cross-functional team (eg, clinical).
Coach or mentor of more junior staff on document planning, processes, and content. Provides peer review as needed.
Active participant in or lead of process working groups.

Qualifications / Requirements:

A university/college degree in a scientific discipline is required. An advanced degree (eg, Masters, PhD, MD) preferred.
At least 6 years of relevant pharmaceutical/scientific; 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.
Able 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 organization.

Johnson & Johnson Family of Companies are equal opportunity employers, and 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 crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

#LI-Hybrid

Required Skills:

Medical Writing, Project Management, Regulatory Writing

Preferred Skills:

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

How we rate this

Medical Writer III, X-TA at Johnson & Johnson rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

●●●● Builds AI80 to 100
●●●○ Works on AI60 to 79
●●○○ Uses AI40 to 59
●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Key facts

Medical Writer III, X-TA is an open job at Johnson & Johnson.
Level rates this role AI Level 1 of 4: Little AI.
The role is based in High Wycombe, Buckinghamshire, United Kingdom.
The job was posted on October 13, 2026.
Seniority: senior.
Applications are handled by Johnson & Johnson. Apply on Johnson & Johnson

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Medical WritingRegulatory WritingClinical Data

Questions you could be asked

Tell me about a project where medical writing was part of your work. What did you do?
Tell me about a project where regulatory writing was part of your work. What did you do?
Tell me about a project where clinical data was part of your work. What did you do?

Adapt your resume

List these exact terms on your resume: Medical Writing, Regulatory Writing, and Clinical Data. An applicant tracking system matches the wording, not the idea.
Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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