DataScience RWE Regulatory Summer Intern

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

With $81.6 billion in 2018 sales, Johnson & Johnson is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. There are more than 250 Johnson & Johnson operating companies employing approximately 130,000 people in 60 countries throughout the world.

Calling all big thinkers and world-changers who want to drive their careers forward across more than 250 leading businesses in consumer, pharmaceutical and medical technology. If you have the talent and desire to touch the world, Johnson & Johnson has the career opportunities to help make it happen. 

Position Components

Janssen Research & Development (“JRD”), a Johnson & Johnson company, is recruiting for summer interns, Janssen R&D Data Science & Digital Health, Real-World Evidence (“RWE”). In this role, you will partner with key businesses across Janssen to apply advanced data science and analytics to answer key research questions.  As an intern, you will get the opportunity to work on cutting-edge problems at the intersection of machine learning and healthcare. You will be a member of a dynamic team comprising data scientists and subject matter experts to create and iterate on data science solutions. You will be exposed in developing, adapting and delivering Real-World Data (“RWD”) methodologies to mitigate observed and unobserved bias and confounding in the execution of comparative effectiveness analyses, time-to-event analyses, external control arm studies, synthetic control arm studies, hybrid control arm studies, observational and prospective study designs, and other use cases; you will also be exposed in generating RWE or secondary evidence from post-hoc RCT analyses, observational databases, and literature reviews to support regulatory and HTA agency interactions including oral and written communications. The primary location for this position is flexible – either; Titusville, NJ; Raritan, NJ; Spring House, PA; Cambridge, MA; New York City, NY; San Diego, CA; South San Francisco, CA; or remote with up to 10% travel.