This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Statistical Programmer based in India.
This role offers the opportunity to contribute to global clinical research initiatives by transforming complex trial data into reliable, regulatory-ready outputs.
The Statistical Programmer will support the creation and validation of clinical datasets that help advance evidence-based healthcare solutions.
You will work with industry-standard programming practices, clinical data standards, and regulatory requirements to ensure high-quality deliverables.
The position combines technical expertise, analytical thinking, and collaboration with cross-functional teams in a dynamic research environment.
You will play an important role in improving data quality, supporting submissions, and enabling accurate clinical safety analyses.
This opportunity is ideal for a detail-oriented programming qualified passionate about clinical research, data standards, and healthcare innovation.
Accountabilities:
The Statistical Programmer will be responsible for developing, validating, and maintaining high-quality clinical trial programming deliverables while ensuring compliance with industry standards. Key responsibilities include:
- Developing, testing, validating, and maintaining SAS programs used to generate clinical trial datasets.
- Producing submission-ready datasets, including SDTM and ADaM datasets, to support clinical safety analyses.
- Creating and maintaining CDISC-compliant data standards and ensuring alignment with regulatory requirements.
- Performing double programming and validation activities to verify the accuracy and reliability of statistical analysis datasets.
- Generating and reviewing compliance checks for SDTM and ADaM formatted datasets.
- Supporting regulatory submission activities by preparing electronic submission packages, Define.xml files, reviewer guides, and related documentation.
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📌 Statistical Programmer (India)
🏢 Jobgether
📍 India
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