Reg Affairs Assoc I
Gilead Sciences · Shanghai, China
OtherFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
What they're looking for
- Strong English verbal and written communication skills
- Bachelor's degree in healthcare management, pharmacy, or life sciences preferred
- 3+ years experience in drug development functions preferred
- Ability to manage multiple concurrent tasks and deliver quality work on schedule
- Cross-functional collaboration skills and proactive team approach
What you'll be doing
- Process timely and accurate payments to NMPA, CDE, and NIFDC for product registrations
- Track and manage functional area budgets, expenditures, invoices, and vendor payments
- Maintain regulatory records, systems, and tracking tools with accurate data entry and reporting
- Coordinate projects and programs aligned with organizational goals and timelines
- Serve as liaison between internal teams, external vendors, and clients for communication and issue resolution
Privacy & handoff
This role links to Gilead Sciences's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.