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EN
简
繁
About Us
Overview
Corporate Information
Board of Directors
Senior Management
Contact Us
Innovation Platform
Overview
R&D Approach
Our Pipeline
Expanded Access
Key Corporate Partnerships
Innovation News
Commercial Platform
Overview
Competitive Advantages
Prescription Drugs
Consumer Health
Commercial Platform News
News & Presentations
Recent News
All RNS & Press Releases
Presentations & Publications
Financial Results
Overview
Chairman's Statement
Financial Highlights
Financial Reports
SEC Filings
Shareholder Information
Overview
Events, Circulars & Forms
Share Price & Chart
Major Shareholders
Analyst Coverage
Dual-listing FAQs
Information for Shareholders
Warning to Shareholders
Terms of Reference & Policies
Audit Committee – Terms of Reference
AIM Rule 26
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Beijing
,
Clinical Operations and Regulatory Affairs
| 11 May 2020
Senior Manager, Regulatory Affairs
Responsibilities
Review product registration dossier and relevant documents
Obtain IND & NDA approval as well as product registration license renewal as planed
Coordinate with each function within HMPL from registration pathway
Establish and maintain relationship with external stakeholders
Liaise with external stakeholders for regulatory needs of HMPL
Implement regulatory activities as required by governmental regulations and internal SOPs
Form accelerate Strategy for product registration
Qualifications
Bachelor degree and above in Pharmacy or Pharmaceutical
5 years or more drug registration experience in pharmaceutical industry
Prefer oncology drug registration background
Good understanding of Chinese pharmaceutical & regulatory environment
Good relation with stakeholders related to product registration
Fluent English
Strong communication skill
Passion in drug development
Apply Now