Intern – Regulatory Affairs
Confirmed live in the last 24 hours
Gilead Sciences

10,001+ employees

Critical disease biopharmaceutical development
Company Overview
Gilead’s mission is to discover, develop and deliver innovative therapeutics for people with life-threatening diseases. The company is committed to creating a healthier world for everyone through their research, development of forward medicines, and clinical trials.

Company Stage


Total Funding





Foster City, California

Growth & Insights

6 month growth


1 year growth


2 year growth

San Mateo, CA, USA
Experience Level
  • Must be at least 18 years old
  • Must have a minimum GPA of 2.8
  • Authorized to work in the United States without Sponsorship now or in the future or CPT/OPT through your University
  • Must be currently enrolled as a full-time student in a Bachelor's/Masters/MBA/PhD/PharmD program at an accredited US based university or college
  • Interns will assist the Global Regulatory Affairs Oncology Liaison team with projects to support department goals and objectives
  • Interns will assist with development and submission of regulatory documents such as clinical study reports, study protocols and protocol amendments, and assist with activities in preparation for annual reporting requirements (e.g., Investigator Brochure, Orphan Annual report, etc.)
  • In addition, the intern work across the global regulatory network on various research projects and present their findings at team meeting and a final poster board presentation at the conclusion of their internship
  • Integrity (Doing What's Right)
  • Inclusion (Encouraging Diversity)
  • Teamwork (Working Together)
  • Excellence (Being Your Best)
  • Accountability (Taking Personal Responsibility)
Desired Qualifications
  • Proficiency with MS Office Suite
  • Ability to identify issues and seek solutions
  • Ability to work both independently and collaboratively
  • Demonstrated commitment to inclusion and diversity in the workplace
  • Efficient, organized, and able to handle short timelines in a fast-paced environment