Global Patient Safety (GPS) Safety Science Fellowship

The BeOne Medicines GPS Safety Science Fellowship is a one-year, post-doctoral training program designed for PharmD graduates seeking to build a meaningful career in drug safety and risk management. This unique opportunity offers hands-on, practical experience within a dynamic, innovative biopharmaceutical environment, combining functional area specialization with cross-functional collaboration across the product lifecycle.

This program is not recruiting for 2027-2028.

At BeOne Medicines, GPS Safety Science plays a critical role in the continuous evaluation of benefit-risk from early development through post-marketing.

The Fellow will be deeply integrated into the Safety Science team, working alongside Product Safety Leads and Safety Scientists. As a Fellow, you will:

Contribute to real-time safety analysis to inform risk mitigation strategies on clinical trials and/or marketed products
Engage in cross-functional collaboration across clinical and regulatory functions to support the development of therapeutic candidates
Gain exposure to product development and safety decision-making at various stages of the drug lifecycle

The Fellow will gain a strong foundation in pharmacovigilance and the scientific, regulatory, and operational acumen needed to thrive in a rapidly evolving biopharmaceutical industry.

Program Structure

The fellowship is designed to cultivate future Safety Scientists through mentorship, project-based learning, and
targeted exposure to core safety activities, including:

Adverse event reporting process, from data collection, case processing, and medical review to regulatory submission of Individual Case Safety Reports
Safety surveillance and signal detection techniques to proactively monitor patient safety
Build technical proficiency in using industry-standard tools, systems, and databases (e.g., EDC, Spotfire, MedDRA, Signal Management System, etc.), which are critical for effective safety data analysis and downstream decision-making
Clinical trial support through authoring of essential clinical research documents and providing strategic safety input into clinical study protocols, Investigator’s Brochure, and Informed Consent Form
Development of safety risk management strategies, including risk minimization and benefit-risk assessment
Engagement in cross-functional safety governance and collaboration with internal and external stakeholders
Exposure to regulatory interactions and global compliance requirements
Contribution to Aggregate Safety Reports (e.g., DSUR, PBRER, etc.)