Nasdaq: $29.30 (+0.06) | AIM: £4.18 (-0.01)
Career Opportunities

HUTCHMED aims 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 Development
Clinical Operations and Regulatory Affairs
General and Administration
Information Technology
Research and Development
Work Location
Hong Kong
Non-China Asia
Other China
Found Related Results: 16
Job Title: Director/Senior Director, Medical Safety Officer, Product Safety & Pharmacovigilance Directly report to: Vice President, Product Safety & Pharmacovigilance Department: Hutchison MediPharma International       Primary
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Job Title: Manager/Senior Manager, Clinical Contracts Job Category: Exempt/Non-Exempt Department/Group: Clinical Operations Job Code/ Req#:   Location: Florham Park, NJ Travel Required: n/a Level/Salary Range: Mgr / Sr. Mgr Position Ty
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Job Title: Global Regulatory Submission Lead Directly report to: Director, Regulatory Operations Department: Hutchison MediPharma (US) Inc.       Position Purpose:  Manages and/or performs all aspects of electronic dossier compilatio
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Job Title: Clinical Pharmacology Scientist Directly report to: Director, Clinical Pharmacology Department: Clinical Pharmacology       SUMMARY OF RELEVANT JOB RESPONSIBILITIES The Clinical Pharmacology Scientist is a scientific and lead
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Key Responsibilities: Be the scientific expert on the assigned therapy area, disease area, clinical practice and competitor landscape; Handling pre-launching, providing professional medical advice in clinical aspect, and medical affairs activiti
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Key Responsibilities: Develop and execute market access strategies and commercialization plan aligned with country objectives; Work across functionally with global and local medical and commercial functions to develop value propositions and mess
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Key Responsibilities: Responsible for analyzing the market of HUTCHMED products and therapeutic areas. Analyze, coordinate and support the information needs of preparing new product launch; Formulate the of marketing strategy and roadmap from pr
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Job Title: Associate Director-Director, Finance Job Category: Exempt/Non-Exempt Department/Group: Finance Travel Required: NA Location: Florham Park, NJ Position Type: Full Time Level/Salary Range: Mid-Level Hiring Manager: Executive Dire
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Job Title: Associate Director-Director, Biostatistics Job Category: Exempt/Non-Exempt Department/Group: Biometrics Travel Required: NA Location: Florham Park, NJ Position Type: Full Time Level/Salary Range: Mid-Level Hiring Manager: Sr. D
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Job Title: Associate Director/Director, Pharmaceutical Program Management Directly report to: Sr. Director, Pharmaceutical Program Management Leader Department: Hutchison MediPharma International Inc.       SUMMARY OF RELEVANT JOB RESPO
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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 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 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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