北京招聘

Role Description

Supports project teams through contributions to product development strategies and the design, planning, execution, analysis, and reporting of clinical studies, with a view toward establishing the conditions essential for determining safety, efficacy, and marketability.

Major Accountabilities

? 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.

Key Performance Indicators

? 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

Education: ? Master degree in statistics or biostatistics

Languages: ? English essential (reading and written)

Experience/Professional Requirement:

? 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

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.