招聘人数:1-2人
到岗时间:不限
年龄要求:不限
婚况要求:婚姻状况
Complete understanding and wide application of technical principles, theories, and concepts in the statistical field.
Independent operational and technical leadership of multiple protocols or non-clinical experiments in one or more therapeutic areas.
Under close supervision, may lead efforts related to project-level activities, to include analyses and inputs into regulatory filings for all phases of development.
Ensure and manage quality, timeliness, and efficiency for all support and deliverables for designated tasks.
Liaise with and provide needed guidance to statistical programmers assigned in support of trial or project deliverables.
Establish and maintain working relationships with relevant team functional representation
Education :
Doctoral degree in statistics or biostatistics. Master’s degree with sufficient relevant experience.
Languages:
Fluent English essential (oral and written)
Experience:
0-3 years with Doctoral degree or at least 5 years with Master’s degree in the pharmaceutical or device industry or equivalent.
Excellent knowledge in statistics and clinical trial methodology.
Sound knowledge of product clinical development and relevance to study design.
Limited or no Health Authority experience.
Excellent written and oral communication.
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