Intern - Kite Development - Global Patient Safety (Pharmacovigilance)

Location: Parsippany, New Jersey, United States. Hybrid internship; work at the designated site is required for the full internship, and fully remote roles are not offered. Relocation may be required.

Hourly compensation: $19.00–$55.00. Eligible employees may also receive housing stipends.

Company

Develop innovative cancer immunotherapies, including CAR-T and TCR-engineered cell therapies, to support durable responses and reduce the burden of chronic care.

What you will do

• Support literature surveillance and targeted reviews of pharmacovigilance and patient safety information.
• Assist with aggregate safety data analyses, safety summaries, tables, presentations, and visualization.
• Support signal detection, signal evaluation, benefit-risk assessment, and safety surveillance strategy activities.
• Review and organize safety information from clinical trials and post-marketing sources.
• Help prepare and maintain DSURs, development safety summaries, safety review materials, and risk management documentation.
• Develop and present a defined summer AI project addressing a pharmacovigilance or drug safety question, along with a final presentation.

Requirements

• Must be at least 18 years old and independently authorized to work in the United States without current or future school or employer sponsorship.
• Must be enrolled full-time at a nationally accredited U.S. college or university and remain enrolled full-time in the following fall semester.
• Current undergraduate, graduate, or doctoral enrollment with a minimum cumulative GPA of 2.8.
• Must commit to a full-time internship lasting 10–12 consecutive weeks between May and August and work at the designated site.
• Interest in pharmacovigilance, drug safety, clinical development, regulatory science, epidemiology, or pharmaceutical medicine.
• Strong problem-solving, organization, communication, and collaboration skills.

Nice to have

• Study in pharmacy, pharmacology, pharmaceutical sciences, public health, epidemiology, biology, medicine, biostatistics, regulatory science, or a related discipline.
• Undergraduate, graduate, MPH, PhD, JD, or PharmD education.
• Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
• Experience or interest in cell and gene therapies, CAR-T therapies, epidemiology, real-world safety surveillance, or regulatory expectations for novel modalities.

Culture & Benefits

• Work with safety physicians, safety scientists, pharmacovigilance professionals, and cross-functional teams.
• Opportunities for professional development, leadership presentations, social networking, and community volunteering.
• Paid company holidays and sick time.
• Housing stipends for eligible employees.
• Culture centered on integrity, inclusion, teamwork, excellence, and accountability.