Full job description
Brief Position Description:
The core responsibility for this position is as a member of the Data Management SAS department at Novotech. The Clinical Data Programmer SAS Trainee (CDP-ST) will be responsible for performing SAS programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP).
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Minimum Qualifications & Experience:
Graduate in Information Technology or Pharmacy or Clinical Research or life science related field or similar. Base SAS Certified with good understanding of Clinical Research terminologies. Awareness about different electronic data capture tools and metadata would be an added advantage.
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Responsibilities:
- The Clinical Data Programmer SAS Trainee will be responsible for SAS programming activities on different projects across different EDC applications in accordance with Novotech standards.
- Perform programming and QC of SAS programs for data listings or reconciliation listings or patient profiles or any other tables/graphs as per specifications for the Data Management group.
- The Clinical Data Programmer SAS Trainee may be requested to design eCRFs and edit checks after necessary training for the respective EDC tools and provide technical support on projects.
- Perform data mapping/reconciliation specifications and programming per the for the respective project. This will also include alpha testing before releasing.
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