IDAR Summer Intern RMW

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld 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 Med Tech, 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

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:

Career Programs

Job Sub Function:

Non-LDP Intern/Co-Op

Job Category:

Career Program

All Job Posting Locations:

Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

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

We are searching for the best talent for IDAR Summer Intern (RMW) to be in Spring House,PA /
Raritan, NJ or Titusville, NJ.

• The Intern term is from May to August, 2027.
• Full time requirement (40 hours per week).
• 3 vacancies are currently available.

Purpose:

The Integrated Data Analytics & Reporting (IDAR) organization within Global Development is seeking highly motivated Summer Interns to join the Regulatory Medical Writing (RMW) function as part of the IDAR Summer Intern Training Academy.

This internship provides an opportunity to gain hands‑on experience in pharmaceutical research and development while learning how Regulatory Medical Writing supports the development, regulatory approval, and maintenance of medicines. Interns will gain exposure to the preparation of high-quality clinical and regulatory documents and learn how scientific, medical, and statistical information is interpreted and communicated throughout clinical development.

The program is designed to provide practical experience, professional development, and exposure to a collaborative pharmaceutical R&D environment.

You will be responsible:

• Supporting Regulatory Medical Writing activities related to clinical development and regulatory documentation.
• Learning how clinical and regulatory documents are developed to support product development, regulatory approval, and product maintenance.
• Supporting the preparation and review of clinical documents, which may include:
• Investigator's Brochures
• Clinical Trial Protocols
• Clinical Study Reports
• Summaries of efficacy and safety
• Responses to Health Authority questions
• Reviewing, interpreting, and summarizing scientific, medical, clinical, and statistical information.
• Applying strong writing and attention to detail to support clear, accurate, and high-quality clinical documentation.
• Gaining exposure to how clinical trial design and study results are translated into regulatory and clinical documents.
• Collaborating with colleagues and cross-functional partners involved in clinical development.
• Participating in assigned projects and learning activities within the IDAR Summer Intern Training Academy.
• Contributing to projects that support the development of medicines within Johnson & Johnson Innovative Medicine.

Qualifications / Requirements:

• Com…