Global Oncology Regulatory Affairs Intern (Hybrid)

Johnson & Johnson Services

United States

Remote

USD 13,000 - 25,000

Full time

8 days ago

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Benefits offered by this job

Mentor program
Poster presentation opportunity

Job summary

Johnson & Johnson Services is offering an Oncology Global Regulatory Affairs internship as part of the Global Oncology Internship Program. The 12-week role runs May 10 to August 13, 2027, with a hybrid on-site three days per week and remote two days.

You will join a global matrixed team, contribute to regulatory strategies, and present your research at a symposium. The program seeks students currently enrolled in a university program, pursuing biology/regulatory/pharma tracks, and who are

Qualifications

  • > Fluent in English, both written and spoken.
  • > Able to work in a global matrixed team.
  • > Strong interest in oncology drug development and regulatory processes.
  • > Must be enrolled in an accredited university program for the duration of the internship.
  • > Able to balance multiple projects in a fast-paced environment.

Responsibilities

  • Glean understanding of clinical research and drug development incl. GCPs, ICH, and SOPs.
  • Attend lecture series to learn the drug development process.
  • Participate in department and cross-functional team meetings.
  • Shadow key functional roles for learning opportunities.
  • Contribute to assigned projects and group activities.
  • Prepare and present an abstract/poster at the annual symposium.
  • Develop or enhance communications, planning, and organization skills in a global virtual team.

Skills

Fluent in English
Leadership
Team collaboration
Regulatory affairs knowledge

Education

Currently enrolled in a university program
Pursuing Bachelor’s/Master’s in biology/regulatory/health sciences

Tools

Microsoft Office Suite (Outlook, Excel, PowerPoint, Word)
Teams
SharePoint

Job description

Johnson & Johnson Services is offering an Oncology Global Regulatory Affairs internship as part of the Global Oncology Internship Program. The 12-week role runs May 10 to August 13, 2027, with a hybrid on-site three days per week and remote two days.

You will join a global matrixed team, contribute to regulatory strategies, and present your research at a symposium. The program seeks students currently enrolled in a university program, pursuing biology/regulatory/pharma tracks, and who are

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