- Provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data
- Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis data specifications
- Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical, statistical reports and other similar reports
- Contribute to the integrated clinical/statistical report and other similar documents
- Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting Perform quality assurance procedures on work performed by others
- Develop, test, validate, document, maintain and execute software and/or systems using the currently endorsed tools or support of production activities
- Assist in the integration of data from remote entry sites, contract organizations and co-licensing partners to the central database
- BA, BS or MS in Mathematics, computer science or Statistics
- Three years of hands-on SAS programming experience in pharmaceutical industry
- Understands the basic skills and goals of reporting clinical data
- Writing knowledge of SAS; SQL and UNIX
- Proven ability to organize workload and priorities and complete tasks on time
- Demonstrated ability to work effectively in a team environment
- Strong interpersonal skills and ability to communicate effectively
- Ability to identify and solve technical problems
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