Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Join us in developing innovative medical documents and support AI-driven healthcare solutions.
- Company: Johnson & Johnson, a leader in healthcare innovation.
- Benefits: Competitive salary, remote work options, and opportunities for professional growth.
- Why this job: Make a real impact on patient care through cutting-edge medical writing.
- Qualifications: University degree in a scientific discipline and relevant medical writing experience.
- Other info: Collaborative environment with a focus on emerging AI technologies.
The predicted salary is between 36000 - 60000 £ per year.
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.
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.
Purpose: Supports the Regulatory Medical Writing AI business lead in delivering the functional AI strategy, including change management support, AI quality improvements, organizing and coordinating user acceptance testing, deployment of upgrades and expansion into new document types. Recent experience authoring basic and complex documents within RegMW scope of work, has working knowledge of document landscape and submission dossiers. Actively participates in or leads process working groups. Provides input into functional tactics/strategy (e.g., writing teams, process working groups). Able to work within document management systems and familiar with workflows. Able to troubleshoot technical issues and collaborate with IT teams.
You will be responsible for:
- Maintains familiarity with current process for development of clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents.
- Assists in rollout and integration of GenAI-enabled authoring and review tools.
- Provides technical and functional support during pilots and full-scale deployments.
- Ensures alignment with regulatory standards and internal SOPs for AI-generated content.
- Supports user acceptance testing and change management activities.
- Develops and delivers training materials for end users.
- Monitors solution performance and gathers feedback for enhancements.
- Maintains current knowledge of emerging AI technologies and regulatory guidance.
- Completes all time reporting, training, metrics database, and project tracking updates as required in relevant company systems.
- Actively participates in or leads process working groups.
Qualifications/Requirements:
Education: Minimum of a university/college degree in a scientific discipline is required. An advanced degree (e.g., Masters, PhD, MD) is preferred.
Skills/Experience: Minimum of 6 years of relevant pharmaceutical/scientific experience is required. Minimum of 4 years of relevant clinical/regulatory medical writing experience is required. Familiarity with AI/GenAI technologies and document automation tools, including prompting strategies. Experience with digital transformation initiatives preferred.
Other: Excellent oral and written communication skills. Attention to detail. Ability to function in a team environment. Organizes time well. Strong leadership skills, both in project and process management as well as in time management (influencing, negotiating, assertiveness, taking initiative). Resolves complex problems under supervision. Demonstrates learning agility. Builds solid and productive relationships with cross-functional team members.
Required Skills:
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).
Medical Writer III,AI-Assisted Operations in High Wycombe employer: J&J Family of Companies
Contact Detail:
J&J Family of Companies Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Writer III,AI-Assisted Operations in High Wycombe
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical writing field on LinkedIn or at industry events. A friendly chat can lead to opportunities you might not find on job boards.
✨Tip Number 2
Prepare for interviews by researching Johnson & Johnson's latest innovations and how they relate to AI-assisted operations. Show them you’re not just another candidate; you’re genuinely interested in their mission!
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience aligns with the role of Medical Writer III. Highlight your familiarity with regulatory documents and AI technologies to stand out.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the team at Johnson & Johnson.
We think you need these skills to ace Medical Writer III,AI-Assisted Operations in High Wycombe
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Medical Writer III role. Highlight your relevant experience in medical writing and any familiarity with AI technologies, as this will show us you’re a great fit for the position.
Showcase Your Skills: Don’t just list your skills; demonstrate them! Use specific examples from your past work that illustrate your expertise in clinical and regulatory documents. This helps us see how you can contribute to our innovative medicine goals.
Be Clear and Concise: When writing your application, clarity is key. Use straightforward language and avoid jargon where possible. We appreciate well-structured applications that get straight to the point, making it easy for us to see your qualifications.
Apply Through Our Website: We encourage you to apply directly through our website. This ensures your application is processed smoothly and allows us to keep track of all submissions effectively. Plus, it’s super easy!
How to prepare for a job interview at J&J Family of Companies
✨Know Your Documents
Familiarise yourself with the types of clinical and regulatory documents you'll be working on, like CSRs and protocols. Being able to discuss these confidently will show your expertise and readiness for the role.
✨Showcase Your AI Knowledge
Since this role involves AI-assisted operations, brush up on your understanding of AI technologies and document automation tools. Be prepared to discuss how you've used these in past roles or how you envision using them in this position.
✨Demonstrate Team Spirit
Highlight your ability to work within a team environment. Share examples of how you've collaborated with cross-functional teams in the past, as this is crucial for success in this role.
✨Prepare for Change Management Questions
Expect questions about change management and user acceptance testing. Think of specific instances where you've led or participated in such initiatives, and be ready to explain your approach and outcomes.
