We are a pharmaceutical group with head office in Hong Kong and looking for professionals who are bright, energetic and service oriented to join us for the following position:

Your responsibilities:

• Project co-ordination and follow up
• Possess deep knowledge and experience in clinical trials and drug registration especially China
• To build up data bank and provide analysis report regularly
• Participate and assist in the research & development field
• Other ad hoc projects as required
• Frequent travel is required

Our expectation:

• University Degree or above in Biology, medical science, chemistry or related disciplines
• Minimum 5 years of experience in related industry
• Native Chinese writing in CFDA applications and fluent English
• Proficient in MS Office (excel, word and powerpoint)
• Meticulous, rigorous and serious in work with effective problem solving technique under time-line pressure  
• Initiative, flexible to work with and also a team player  

Please forward your detailed resume with present and expected salary by clicking "Apply Now".

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