IDAR Regulatory Medical Writing Intern (Summer)

6084-Janssen Research & Development, LLC Legal Entity; Spring House (PA); Hybrid; USD 32,000 - 72,000; Full time

Benefits offered by this job

Health benefits

Job summary

Johnson & Johnson’s IDAR Summer Intern program in Spring House PA / Raritan NJ / Titusville NJ offers hands-on Regulatory Medical Writing experience within the IDAR Trainee Academy. You will develop high-quality clinical and regulatory documents, learning how data translates into regulatory submission documents.

The role is a 2027 May–August internship (40 hours/week) with opportunities to collaborate across cross-functional teams and gain exposure to medicines development in a global pharma

Qualifications

• Enrollment in accredited university for the duration of the internship.
• Pursuing Bachelor's/Master's/PharmD/PhD in related fields; GPA 3.5+.
• Hybrid schedule with at least 3 days/week on-site in NJ/PA.
• Authorized to work in the U.S. without visa sponsorship.
• CPT/OPT/STEM OPT may affect eligibility.

Responsibilities

• Support Regulatory Medical Writing activities related to clinical development.
• Assist in preparing and reviewing clinical documents (IBs, protocols, CSR, summaries).
• Review and summarize scientific, medical, and statistical information.
• Collaborate with cross-functional teams in clinical development.
• Gain exposure to trial design translation into regulatory documents.

Skills

Written communication

Attention to detail

Time management

Cross-functional collaboration

Presentation skills

Independent work

Education

Biological sciences degree

Job description

Johnson & Johnson’s IDAR Summer Intern program in Spring House PA / Raritan NJ / Titusville NJ offers hands-on Regulatory Medical Writing experience within the IDAR Trainee Academy. You will develop high-quality clinical and regulatory documents, learning how data translates into regulatory submission documents.

The role is a 2027 May–August internship (40 hours/week) with opportunities to collaborate across cross-functional teams and gain exposure to medicines development in a global pharma