Global Regulatory Affairs (GRA) Fellowship

View Our 2026-2027 Brochure

The GRA Fellowship program is a one-year rotational program consisting of the following rotations:

Global Regulatory Policy and Intelligence (GRPI)

• The GRPI team analyzes and presents the latest in health authority regulatory trends, policy initiatives, and approvals across therapeutic areas.
• The fellow will learn how timely and thorough analysis of nuances of regulatory precedents along with tracking dynamic regulatory environment is essential to successful drug development.

Regulatory Advertising and Promotion

• The regulatory advertising and promotion team administers the promotional review process, prepares FDA submissions for promotional materials, and provides regulatory review and oversight for promotional and non-promotional product communications
• The fellow will learn about FDA regulatory requirements for promotion and other product related communications

Regulatory Strategy

• The regulatory strategy team plans and coordinates regulatory submissions and provides guidance to the cross- functional development teams on regulatory strategy and tactics
• The fellow will support the regulatory affairs lead(s) with developing and implementing strategies for optimal regulatory development of BeOne pipeline drug development programs

Global Labeling

• The labeling team develops and maintains global core labeling for commercial products and provides regulatory support for local labeling development and implementation.
• The fellow will learn about regulatory labeling strategy and operations, and support activities for management and governance of global and local product labeling.

This program requires a Pharm.D., relevant Ph.D. in life sciences, or Master’s in Regulatory Affairs completed by July 2026.

Qualified candidates must be legally authorized to be employed in the United States at the time of application without BeOne sponsorship.

• To apply, please email GRAFellowship@beonemed.com by October 15, 2025, the following initial application materials:
• • Curriculum Vitae (CV)
  • Letter of Intent
  • Unofficial College Transcript
• If selected for an interview the following advanced application materials will be requested by email:
• • Writing Sample (no more than 2 pages; eg, poster or journal abstract, etc.)
  • Three (3) Letters of Recommendation
• Candidates selected for the final round of interviews will be asked to deliver a short presentation on a regulatory topic, which will be provided in advance.
• Submission prior to the deadline is strongly encouraged.
• Please address letters of recommendation and letters of intent to:
• • Danielle Ziernicki, BS, PharmD, RPh
    Head, Global Regulatory Policy and Intelligence
    BeOne Medicines

For any questions, please contact GRAFellowship@beonemed.com.