Statistical Programmer
On-siteCoimbatore, Tamil Nadu, India
Job Summary
Import and export raw data, contribute to mapping specifications for SDTM and client-specific domains, and utilize SAS, R, or Python programming skills for clinical trial study submissions. Develop programs identifying data issues, debug custom functions and macros, and ensure datasets comply with CDISC standards and regulatory guidelines. Understand CRF annotations, check consistency with raw data, and communicate with internal teams to create deliverables for pharmaceutical and CRO clients while working in tandem with Biostatistics and Data Management members. Follow client processes, SOPs, and company policies to support quality control and team metrics.
Required Qualifications
- Clinical Domain knowledge
- Familiarity with CDISC Standards (SDTM Knowledge, ADaM, Submission package)
- SAS Programming (Experience up to 2 years)
- Graduation in Pharmacy/Computer Science, or any such equivalent graduation from a reputed institute
- Total experience is between 2 - 4 years
Desired Qualifications
- Python Programming will be an added advantage
- R Programming will be an added advantage
- Good Communication skills, learning attitude and good team player
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