Career Opportunities

Chi-Med’s aim is to become a major pharmaceutical company developing innovative drugs for both the Chinese and global markets. We invite motivated individuals to join our team. In return for your talent and enthusiasm, we are committed to providing a challenging and collaborative work environment that is both rewarding and fulfilling. If you are up for the challenge, please send us your resume.

Function Team Filter
Business Development
Clinical Operations and Regulatory Affairs
General and Administration
Research and Development
Work Location
Hong Kong
Non-China Asia
Other China
Found Related Results: 12
Responsibilities Building strong relationships internally and externally with all key stakeholders in the collaboration. Partner with steering committee members involved in collaborations to resolve issues and help embed partnering best practices
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Acting as one of the core team members in HMP New DP Plant Project, provide frontline participation in the design, development, qualification and validation of GMP related systems, including laboratory areas meeting cGMP requirements from China, U
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Responsibilities Prepare process R&D related documents and reports to support IND and NDA. Update technical documents and effectively communicate with process R&D team. Support process R&D team to provide documentation for IND, NDA, I
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Responsibilities Performance Management: Performance management and analysis - Tracking business performance, measuring variance to plan / KPI-targets & driving corrective actions. Performance Meetings and Business reviews - Communicating Ins
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Responsibilities Provide medical input to marketing product team in product positioning and develop publication plan and clinical research proposal for the defined therapeutic areas Provide medical inputs in developing training program on disease
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Primary Duties Management of clinical research project. Vendor (CRO, Lab, drug storage, etc.) supervision and management. Liaison with KOLs. Support IND and NDA filing. Quality control of the clinical research projects, such as co-monitoring.  
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Primary Function The Statistical programmer/Senior Statistical Programmer is responsible for all statistical programming aspects at project level. The position is a key contributor with biostatistics in ensuring that pharmaceutical drug-developmen
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Responsibilities: High profile discovery-and-development toxicology leadership role for design, implementation, interpretation and reporting safety profiles for small molecule therapeutics, including IND- and Phase III-enabling toxicology studies
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Responsibilities Play as one of the key brand team members Involve to develop the brand plan / product strategies Develop, review and approve promotional materials Proactively share the latest medical information including clinical trial data, ne
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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
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Primary function: Product registration   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 fro
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Primary Function Primary leader oversees overall development strategy, and execution accordingly Take lead in Clinical Development Activities related to products, protocols or studies. Serve as a scientific, medical accountable person for quality
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