Ctry Approval Spec
Thermo Fisher Scientific · Beijing, China
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Role summary
Country Approval Specialist position supporting clinical trial startup activities at Thermo Fisher Scientific's PPD clinical research services in Beijing. Manages and coordinates regulatory submissions, provides local strategy guidance, and ensures alignment between submission and site activation timelines.
What they're looking for
- Bachelor's degree or equivalent formal academic or vocational qualification
- Knowledge of local regulatory submission processes and requirements
- Understanding of clinical trial regulatory guidelines and company SOPs
- Project coordination and stakeholder management experience
- Attention to detail and ability to maintain accurate documentation
What you'll be doing
- Prepare, review, and coordinate local regulatory submissions aligned with global strategy
- Provide regulatory strategy advice to internal clients on Ministry of Health and Ethics Committee matters
- Coordinate site startup services and ensure alignment with submission timelines
- Serve as key country-level contact for regulatory and ethical submission activities
- Maintain trial status information in tracking databases and manage study files per company standards
Privacy & handoff
This role links to Thermo Fisher Scientific'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.