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| Contract Title: |
Statistical Programmer - U.K.and
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| Contract Description: |
Accountabilities/Responsibilities: and#x2022;Provide support to the statistical programming team on activities related to analysis and reporting of assigned drug development study data. and#x2022;Perform trial protocol and Case Report Form (CRF) review. Create data structures definitions including CRF annotations for clinical trials. Ensure consistency and adherence to available standards. and#x2022;Perform the user acceptance testing of data structure provided to PDIB by Data Management and execute data quality acceptance checks. Develop additional study-specific checks as required. and#x2022;Interact with members of the statistics and statistical programming team to clarify requirements. and#x2022;Contributes to programming specifications for analysis datasets (VADs), listings, tables, and figures under guidance of a senior team member. and#x2022;Program, validate and document VADs, listings, tables, and figures for clinical trials according to the agreed specifications, with high quality and within agreed time lines. and#x2022;Adhere to statistical programming standards, effectively use available standard programs, ensure availability of appropriate documentation and comply with Standard Operating Procedures. and#x2022;Execute electronic submission process if applicable. and#x2022;Support senior member of the statistical programming team in maintaining efficient interfaces with internal and external customers. and#x2022;Support statistical programming group in implementing user aspects of improvement initiatives, especially with respect to statistical programming and technical implementations of data processing as well as analysis and reporting procedures. and#x2022;Contribute to internal training related to statistical programming activities. Essential Skills and Capabilities: and#x2022;University education or equivalent in Mathematics, Statistics, Computer Science or other analytical field. and#x2022;At least 3 years of pharmaceutical industry drug development experience using SAS. and#x2022;Good knowledge of SAS programming language, level of proficiency with SAS/Base, SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS. and#x2022;Good knowledge of English in a business environment. and#x2022;Basic knowledge of drug development process in particular on collection, storing, processing and analysis of clinical trial data. and#x2022;Knowledge and in Data base interfaces and programming experience in a UNIX operating system are considered a distinct advantage. Send your Application for this Contract by using the 'Apply' link below. |
| Contract Location: |
U.K.and |
| Contract Salary: |
75 per hour |
| Contract Type: |
Contract |
| Contract Start: |
asap |
| Contract Duration: |
12 months |
| Warning :- Before applying for the Statistical Programmer U.K.and Contract , It
is unlawful to employ a person who does not have permission
to live and work in the UK. Please ensure you already have this permission. |
Click Here to Apply
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