パレクセルでの仕事
パレクセルは、臨床開発の上流から下流までのそれぞれの専門領域で、国内外の多くのお客様に高度なソリューションを提供するプロフェッショナル集団です。 パレクセルは、新しい薬や治療法を、それらを必要としている人々にいち早く届けることを目指し、日々の業務に取り組んでいます。
Senior Associate
応募 求人ID R0000038785 ロケーション 北京市, Beijing Shi 仕事内容1 Contribute to delivery of regulatory intelligence and pharmacovigilance (PV) regulatory intelligence for Mainland China and Taiwan.
- Deliver consolidated regulatory intelligence for Mainland China and Taiwan, in accordance with company expectations.
2 Regulatory/PV Regulatory Impact Assessment & Stakeholder Engagement
- Monitoring and analysis of regulatory updates (including laws, guidelines, technical requirements, and trends) issued by the NMPA, CDE, TFDA and other relevant regulatory bodies in Mainland China and Taiwan
- In conjunction with local GRAS SMEs, provide a local assessment/interpretation of new/revised regulatory information and triage for a global impact assessment according to company SOPs
- Manage global impact assessments of new/revised regulatory information for Mainland China and Taiwan according to company SOPs
- In conjunction with local PV SMEs, provide a local assessment/interpretation of new/revised PV regulatory intelligence and triage for a global impact assessment according to company SOP.
3 Regulatory Policy: Intelligence Analysis & Support
- Provide intelligence analyses and support for regulatory policy priorities (e.g., major legislative changes with direct impact on CSL).
- Track regulatory policy updates trends issued by the NMPA, CDE, and other relevant regulatory bodies in Mainland China and Taiwan.
- Provide strategic input to company SMEs by curating impact assessments, including evaluating potential impacts on technical and procedural requirements and translating these into actionable insights.
- Support policy activities by providing preliminary analysis of regulatory challenges and opportunities and insights on how to mitigate risks or capitalise on opportunities
- Provide analyses according to company processes and using company templates.
Maintain structured regulatory intelligence tracking to ensure timely awareness of emerging regulatory signals.
4 Global-Local Regulatory Alignment & Liaison
- Liaise with local and global GRAS teams/SMEs, clinical, medical affairs, and quality assurance SMEs to ensure alignment on impact assessment activities.
- Advise internal regulatory teams and GRASP Regional Lead on evolving regulatory expectations.
- Ensure alignment between country-specific regulatory intelligence and the company’s global regulatory intelligence/impact assessment framework.
5 Regulatory Intelligence Infrastructure Management
- Develop, maintain, and optimize regulatory intelligence databases, trackers, and internal communication channels.
- Ensure all regulatory intelligence activities adhere to the company’s internal governance policies and compliance standards.
- Support the preparation and conduct of PV inspections and audits, as requested.
