南京招聘

Roles and Responsibilities:

1. velops standards SAS Code (programs and macros) that are used across all TAs or used within a specific TA. This includes but is not limited to

• Performing comprehensive review of project requirements
• Designing the code implementing the statistical requirements
• Developing and unit testing SAS Code
• Developing User Acceptance Testing (UAT) based on test data set repository
• Performing code reviews
• Executing UAT and Reporting accurately findings
• Developing documentation

• Maintains standards SAS code.
• Performing impact analysis based on changed input requirements (SDTM, Analysis Rules, ADaM) or changed output requirements (AD data sets, displays)
• Translating impact on standards sas code into plan of action for updating the code
• Developing and performing unit testing and user acceptance testing.
• Maintaining documentation
• Applies expertise and problem-solving skills to complete robust analysis standards programming activities of high complexity and ambiguity benefitting multiple project teams
• Provides input into, project requirements and/or project documentation
• Collaborates effectively within standards team and statistical programming, and with cross-functional working group team members, including internal and external members.

Skill sets

Required

·         SAS programming expertise, specifically proven record in robust multi-purpose macro development

·         Expertise in interpreting the CDISC foundational standards, especially ADaM but also SDTM, Controlled Terminology and Define.xml

·         Expertise in various trial designs, statistical analysis and reporting activities and approaches across therapeutic areas and clinical phases

·         Handle multiple tasks and prioritize accordingly

·         Track record of delivering according to plan

·         Has excellent communication skills, verbal and written

·         Can work autonomously in a cross functional environment

Desired

• Cross Therapeutic Area experience
• Global work experience
• Experience with biomedical concepts is a plus.

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.