Description
Standard AnalystFUNCTION DESCRIPTION
Our global pharmaceutical client is looking for a Standard Analyst (SSA) to work within the standard team with previous experience in clinical data management and SAS programming. He/she will have to design screens in central designer (InForm) and will have to write edit checks in the same system.
KEY RESPONSIBILITIES
o Set-up and validation of data entry screens (eCRF design, workflow rules) in InForm (Central Designer)
o Maintenance of libraries in Central Designer (InForm)
o Programs/validates edit checks in InForm (Central Designer)
o Manages validation plans and validation execution with external partners
o Manages extraction mapping
o Documentation of InForm standard application (Study book, TE schedule, IDRP, validation plan, etc..)
o Completion of study environmental data
o Writing specifications for SAS data checks and listings
o SAS programming and validation of data checks and listings
o Provide support to study set-up activities
o Project workload management and supervision of project programmers
PREREQUISITES
o SAS programming
o SAS macros
o SQL
o InForm (Central Designer) would be an asset
o Experience in clinical data management
o Strong experience in SAS programming (minimum 3-5 years experience)
o Experience in InForm would be an asset