Jobs Location:New London, Connecticut
Create submission-ready standard data presentations and data sets usingstandard coding and following standard industry processes including SDLC
Creating SAS programs and producing outputs to support the analysis andreporting of clinical trials.
Developing analysis datasets for trial level reporting by following theAnalysis Data Model (ADaM).
Programming standard and custom data listings, summary tables, and graphs asspecified in statistical analysis plan
Extract the data from clinical database for data reporting purpose.
Develop programming specifications by analyzing the protocol related documents.Meet the programming requirements for submissions as required
Understand and plan work to delivery timelines including allowing time forinternal QC, as appropriate
Whenever required, collaborate with the statistician, data managers, andclinicians to resolve specifications and data related issues.
Work with supervisor to balance conflicting priorities
Understand timelines for and milestones affecting their work and alertsupervisor and client representative to potential slippage
Run routine QC programs, track the changes in programming and specifications,and document the QC results and resolutions. Carry out rework as requested by supervisor or client representative
Follow escalation process and neither suppress nor over- escalate issues
Contribute to close –out evaluations and any discussion
Ensure compliance with Eliassen and industry quality standards, guidelines andprocedures
Other duties as assigned.
Please email your resume to firstname.lastname@example.org
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