Statistical Programmer Ii

2 days ago

Coimbatore, India Algorics Full time

**Job Components / Major Responsibilities**:
This job description serves only to give a broad outline of the duties required and will be renewed and amended at periodic intervals.
- Performs all SAS programming required for analysis and reporting.
- Plan, write and execute SAS programs designed to analyse clinical trial data, including any or all of the following: analysis datasets, tables, listings and graphs.
- Coordinate, create and maintain programming project documentation.
- Validate and perform quality control checks on programming.
- Maintains high productivity on projects and seeks input to increase efficiencies if needed.
- Maintain, verify, and ensure the quality and accuracy of all assigned work.
- Anticipate and communicate resource and quality issues that may impact deliverables or timelines to project team leader.
- Work with Biostatistics and Data Management to resolve issues regarding the interpretation and reporting of data.
- Comply with all applicable regulatory requirements, company standards and procedures.
- Identify and solve technical problems and work independently on assigned tasks.
- Assist with the transfer of deliverables to either internal or external sponsors.

**Qualifications**:

- Bachelor’s degree in Statistics/Mathematics/Computer Science or life science
- At least three years of experience as SAS programmer for all clinical trial phases and demonstrate the ability to independently perform SAS programming.
- Proficient in industry standards, CDISC data standards, ICH-GCP guidelines, medical terminology, and clinical trial methodologies.

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