IDAR Summer Intern - RMW

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:
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:

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

Johnson & Johnson is currently recruiting Summer Interns for our Integrated Data Analytics and Reporting (IDAR) Summer Intern Training Academy!  We are recruiting for the following department: Regulatory Medical Writing (RMW).

The positions are for university undergraduate students who will be entering their junior or senior year, or graduate students who will continue their postgraduate program after the internship.

We are seeking highly motivated candidates to join our Summer Intern Training Academy.

The Academy is a premier training program focused on developing and inspiring talent considering a career in pharmaceutical research and development.

You can gain hands-on experience and help advance our medicines in development at Johnson & Johnson.

Remote work options may be considered on a case-by-case basis and if approved by the Company.

 

As an intern in the RMW department, you have the opportunity to learn how to write high quality clinical documents to support the development, regulatory approval, and maintenance of our products.

These documents include investigator’s brochures, clinical trial protocols, and clinical study reports, as well as summaries of efficacy and safety and responses to health authority questions.

How you can make a difference: Apply your excellent writing skills, ability to interpret and summarize statistical and medical information and attention to detail to the design of our clinical trials and reporting of our data.

Qualifications:


* Candidates must be legally authorized to work in the U.S.

and must not require sponsorship for employment visa status now, or in the future (e.g., H1‑B).


* Candidate must be actively enrolled in an accredited University for the durati...