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 https://www.jnj.com

Job Function:

Medical Affairs Group

Job Sub Function:

Medical Writing

Job Category:

Professional

All Job Posting Locations:

Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, US159 NJ Titusville - 1125 Trenton-Harbourton Rd

Job Description:

Analyst, Regulatory Medical Writing

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

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-008756
• EU (e.g., Belgium, Finland, France, Germany, Netherlands) - Requisition Number: R-009077
• Switzerland – Requisition Number: R-009084
• United States - Requisition Number: R-009090
• Canada - Requisition Number: R-009088

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

This is a hybrid or remote role available in all locations within Europe and North America. While specific cities are listed in the locations section for reference, please note that they are examples only and do not limit your application. We invite candidates from any location to apply. Remote work options may be considered on a case-by-case basis and if approved by the Company.

We are searching for the best talent for Analyst, Regulatory Medical Writing.

As Analyst, Regulatory Medical Writing, you will support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, and Specialty Ophthalmology). Within our Regulatory Medical Writing team, you will join a cohort of writers undergoing internal training to author diverse regulatory medical writing documents. The target start date is 1 September 2025.

Purpose:

• Learn the regulatory medical writing role and pharmaceutical industry and business.
• Learn to work in a team environment and matrix.
• Learn internal standards, regulatory, and publishing guidelines.
• Learn internal systems, tools, and processes.
• Help to prepare sections of documents and prepare basic documents under supervision.
• Assist with routine tasks per established procedures.

You will be responsible for:

• Prepare components of clinical and regulatory documents and write basic documents such as tables of studies, narratives, protocol amendments, investigator’s brochure updates and addenda under supervision.
• May assist with document QC, abbreviations, references, literature searches, and other tasks.
• Learn how to interpret, summarize, and present statistical and medical information.
• Learn to work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
• Attend cross-functional meetings with other writers as appropriate (eg, project kick-off and review meetings).
• Learn and adhere to SOPs, templates, best practices, policies, and Medical Writing Style Guide.
• Regularly meet with manager and mentors and attend departmental meetings.

Qualifications / Requirements:

• A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master’s degree, PhD, MD) preferred.
• Strong oral and written communication skills in English.
• Ability to understand and summarize scientific data.
• Ability to function in a team environment and to build solid and positive relationships with co-workers.
• Demonstrated problem-solving skills.
• Attention to detail.
• Organizational skills and time management skills.
• Demonstrated learning agility.
• Ability to learn and apply knowledge of regulatory guidance documents such as ICH requirements.
• Working knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).

For United States Applicants only:

The anticipated base pay range for this position is $88,400 to $119,600.

The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/ performance year. Bonuses are awarded at the Company’s discretion on an individual basis.

Employees and/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Employees are eligible for the following time off benefits:

• Vacation - up to 120 hours per calendar year
• Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
• Holiday pay, including Floating Holidays - up to 13 days per calendar year
• Work, Personal and Family Time - up to 40 hours per calendar year

For additional general information on company benefits, please go to: https://www.careers.jnj.com/employee-benefits

The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

#LI-Hybrid

#LI-Remote

The anticipated base pay range for this position is :

88,400 - 119,600 USD

Additional Description for Pay Transparency:

Push the boundaries of science to transform health—and your career.

Join us and advance life-changing treatments for people who need them most. At Johnson & Johnson, our focus is on improving global health equity and developing MedTech and pharmaceutical innovations that impact the future of health. Using AI and robotics to transform surgery or helping data scientists and clinicians formulate new ways to diagnose and treat disease, this work may sound like sci-fi, but it’s all science, all real, and could be your career. Whatever your background, skills, or career goals, there’s a place for you to help solve some of the world’s most pressing health challenges with us.

Accelerate your career while changing the world.

Each of our broadly-based family of companies offers an inclusive and empowering culture and employee benefits (like paid time off to volunteer, transgender-inclusive and same-sex partner health insurance coverage, and more) designed to help you live your best life, however you define it. And our best-in-class learning and development approaches, mentorship, and access to innovators across the world will help you grow your skills and reach your career goals. Because when you're at your best, nothing stands between you and your next breakthrough.