Statistical Programmer
Opella Healthcare Group (company site, opens in a new tab)3–6 yrsHyderabadOn-siteDirect career pageEst. 10–18 LPA
Posted 8h ago
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Job description
Structured overview of role & requirements
About This Role
- Implement statistical analysis plans and produce QC’d tables, figures, and listings for clinical publications and ad-hoc requests.
- Develop, implement, and document advanced SAS macros and non-routine programming techniques.
- Collaborate with Medical Affairs biostatisticians and internal teams to ensure SOP compliance, meet timelines, and maintain quality standards.
Minimum Requirements
- Master's degree with 2-3 years or Bachelor’s degree with 3-6 years of relevant statistical programming experience.
- Advanced SAS programming skills mandatory.
- Experience with SDTM and ADaM (CDISC standards) required.
- Excellent written and spoken English language skills.
Ideal Candidate Profile
- Experience working closely with biostatisticians and Medical Affairs stakeholders in clinical trial data analysis and programming.
- Proven ability to manage timelines and deliverables independently while maintaining documentation and quality control.
- Familiarity with global biostatistics programming team processes and adherence to SOPs in pharmaceutical or clinical research environment.