IDAR Summer Intern (RMW)
Johnson & Johnson
Johnson & Johnson seeks motivated summer interns for the Regulatory Medical Writing function within Integrated Data Analytics & Reporting. Interns will gain hands-on experience supporting clinical development documentation, regulatory submissions, and scientific communication during a May-August 2027 program across Pennsylvania and New Jersey locations.
Responsibilities
- Support regulatory medical writing activities for clinical development and regulatory documentation
- Assist with preparation and review of clinical documents including protocols, reports, and regulatory submissions
- Review and interpret scientific, medical, clinical, and statistical information for documentation
- Collaborate with cross-functional teams involved in clinical development
- Participate in assigned projects within the Summer Intern Training Academy
Requirements
- Completed freshman year at accredited university; actively enrolled pursuing Bachelor's, Master's, PharmD, or PhD
- Cumulative GPA of 3.5 or higher across all college coursework
- Permanent U.S. work authorization; no visa sponsorship required now or in future
- Strong written communication skills and attention to detail
- Ability to review, interpret, and summarize scientific, medical, and statistical information
- Capacity to work hybrid schedule with minimum three days weekly on-site in New Jersey or Pennsylvania
$23.5 per hour
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