Regulatory Medical Writing Intern - Summer

Johnson & Johnson

Titusville (NJ)

Hybrid

USD 32,000 - 72,000

Full time

14 days+

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Benefits offered by this job

Company-sponsored medical benefits
Pension plan

Job summary

Johnson & Johnson invites students to join the IDAR Summer Intern Training Academy as a Summer Intern in Regulatory Medical Writing. The role spans Spring House, Raritan, or Titusville locations with a May–August 2027 term and a 40-hour workweek.

Interns assist in clinical and regulatory documentation under guidance, developing scientific writing and regulatory understanding. The program emphasizes hands-on experience in pharmaceutical R&D, exposure to regulatory documents, and collaboration

Qualifications

  • Strong written communication skills.
  • Ability to review, interpret, and summarize scientific information.
  • GPA 3.5 or higher across college coursework.

Responsibilities

  • Support Regulatory Medical Writing activities related to clinical development and regulatory documentation.
  • Learn how clinical/regulatory documents support product development and regulatory approval.
  • Assist in preparing and reviewing clinical documents such as Investigator's Brochures, Protocols, and Clinical Study Reports.
  • Summarize efficacy and safety data and respond to Health Authority questions.
  • Collaborate with cross-functional teams within IDAR Summer Intern Training Academy.

Skills

Written communication
Attention to detail

Education

Pursuing Bachelor/Master/PhD in Biological Sciences or health-related fields

Job description

Johnson & Johnson invites students to join the IDAR Summer Intern Training Academy as a Summer Intern in Regulatory Medical Writing. The role spans Spring House, Raritan, or Titusville locations with a May–August 2027 term and a 40-hour workweek.

Interns assist in clinical and regulatory documentation under guidance, developing scientific writing and regulatory understanding. The program emphasizes hands-on experience in pharmaceutical R&D, exposure to regulatory documents, and collaboration

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