Medical Writer III

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.

We are searching for a Medical Writer III within our Regulatory Medical Writing team, part of Integrated Data Analytics & Reporting (IDAR), to support our Immunology therapeutic area. This hybrid position (3 days per week onsite, 2 days remote) may be located in Spring House, Raritan, Titusville, Horsham (United States) or in the United Kingdom, Netherlands, Belgium, or Switzerland. Remote work options may be considered on a case-by-case basis if approved by the company.

• Write or coordinate clinical and regulatory documents such as CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents.
• Lead cross‑functional document planning and review meetings, coordinating with clinical and other functional teams.
• Interact with cross‑functional colleagues on content, champion medical writing processes and best practices, and establish document timelines and strategies in accordance with internal processes.
• Complete all time‑reporting, training, metrics database, and project‑tracking updates as required in company systems.
• Serve as the primary point of contact for medical writing activities for the cross‑functional team.
• Coach or mentor junior staff on document planning, processes, and content, and provide peer review as needed.
• Actively participate in or lead process working groups.

• A university or college degree in a scientific discipline (advanced degree such as Masters, PhD, or MD preferred).
• At least 6 years of relevant pharmaceutical or scientific industry experience, including at least 4 years of regulatory medical writing experience.
• Strong experience in the Immunology therapeutic area preferred.
• Proficiency in interpreting, summarizing, and presenting statistical and medical information to ensure quality and accuracy of content in complex document types under general supervision.
• Leadership skills in project and process management, time management, influence, negotiation, and initiative.
• Strong attention to detail, learning agility, and mentoring competency.
• Excellent written and spoken English and the ability to collaborate with global teams across time zones.

• Cross‑functional partnership and collaboration
• Lead work and project management
• Medical writing and regulatory writing

• 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 orientation, proofreading
• Quality standards, research ethics, standard operating procedure (SOP)

For United States applicants, the anticipated base pay range for this position is $109,000 to $174,800. The position is eligible for an annual performance bonus and a comprehensive benefits package that includes medical, dental, vision, life insurance, disability insurance, accident insurance, legal insurance, retirement plans (401(k)), vacation, sick time, holiday pay, and other time‑off benefits. Candidates hired outside the United States will receive compensation and benefits in accordance with their local market.

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