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
Manufacturing
Research and Development
Work Location
Beijing
Europe
Hong Kong
Non-China Asia
Other China
Shanghai
Suzhou
USA
Found Related Results: 10
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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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. &n
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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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The primary function for this position is to manage registration related daily activities for Pharmaceutical Sciences, such as China’s and US IND, NDA, EU IMPD, MAA documents writing and tracking. Responsibilities Participate in establishing re
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The primary function for this position is to oversee analytical development’s daily activities, such as method development and validation, analytical testing and stability program. Responsibilities Supervise a group of analytical development sc
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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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