sas-job
Base:shanghai
Requirements:
1. Qualification
Post-Graduate / Ph.D. degree in Statistics
Over 4 – 8 years of experience as a biostatistician for global clinical trial submissions to regulatory authorities like FDA, EU.
Fluent English + reading and written level Japanese.
2. Special Skills and Knowledge
-Clinical Research
-Good Statistical Practice
-Design of clinical trials (concept protocol)
-Sample size estimation
-Randomization
-Statistical programming with tools like SAS
-Handled activities at project/molecule level – development of Statistical analysis plan and other project documents like Master analysis plan
公司为世界知名500强外资公司,全球4万多员工,在世界各地有研发中心,完善的福利及培训制度,有班车,每天定点上下班。英日双语工作环境。
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Email & Msn: sunshine_0708@live.cn