Regulatory Medical Writing Summer Intern (IDAR)

Johnson Johnson

Spring House (PA)

Hybrid

USD 21.000 - 34.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Johnson & Johnson Innovative Medicine seeks IDAR Summer Interns (RMW) to be in Spring House, PA / Raritan, NJ or Titusville, NJ. The Intern term is May to August, 2027. Full time requirement (40 hours per week).

3 vacancies are currently available. The Integrated Data Analytics & Reporting (IDAR) organization within Global Development offers hands-on experience in Regulatory Medical Writing, helping prepare high-quality regulatory documents and learning how clinical and statistical information

Qualifikationen

  • Completion of Undergraduate Freshman year is required.
  • Active enrollment in an accredited university for the duration of the internship.
  • Pursuing a Bachelor's, Master's, PharmD, or PhD in related fields with a GPA 3.5+.
  • Ability to work in a hybrid schedule with three days per week on-site in NJ or PA.

Aufgaben

  • Support Regulatory Medical Writing activities related to clinical development and regulatory documentation.
  • Learn how clinical and regulatory documents are developed to support product development, regulatory approval, and product maintenance.
  • Assist in the preparation and review of documents such as Investigator's Brochures, Protocols, and Study Reports.
  • Review, interpret, and summarize scientific, medical, and statistical information with strong attention to detail.

Kenntnisse

Strong written communication
Ability to review and summarize
Attention to detail

Ausbildung

Bachelor's degree in progress in Biological Sciences/Health-related field

Jobbeschreibung

Johnson & Johnson Innovative Medicine seeks IDAR Summer Interns (RMW) to be in Spring House, PA / Raritan, NJ or Titusville, NJ. The Intern term is May to August, 2027. Full time requirement (40 hours per week).

3 vacancies are currently available. The Integrated Data Analytics & Reporting (IDAR) organization within Global Development offers hands-on experience in Regulatory Medical Writing, helping prepare high-quality regulatory documents and learning how clinical and statistical information

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