Ref #: 25118

Employment type: Permanent - Full-Time

Location: Beijing


• Understand theories, and concepts in statistical field.
• Be responsible for study design/ data analysis in one or more franchises.
• Ensure and manage quality, timeliness, and efficiency for designated tasks.
• Liaise with and provide needed guidance to statistical programmers assigned in support of trial or project deliverables.
• Establish and enhance work relationships with relevant team representative.
• Understanding and wide application of statistical principles, theories, and concepts.
• Ensure quality and timeliness of all deliverables for projects.
• Compliance with internal and external standards as measured by audit findings.
• Works under close supervision of supervisor or project statistician who is responsible for the overall statistical design strategy of the project.

Ideal Background
•Master degree in statistics or biostatistics
•Fluent English essential (reading and written)
•2 years relevant experience in pharmaceutical industry or 1 year in medical device industry
•Programming experience in SAS and R
•Excellent knowledge in statistics and clinical trial methodology
•Better with knowledge of clinical evaluation report and oversea CSR justification routes for registration
•Excellent written and oral communication skills