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2.0 - 3.0 years
2 - 11 Lacs
thiruvananthapuram, kerala, india
On-site
What You Will Be Doing: Assisting in the development, validation, and maintenance of statistical programs (SAS, R, or similar) for data manipulation and analysis in clinical trials. Collaborating with senior statistical programmers and biostatisticians to understand project requirements and contribute to statistical analysis plans (SAPs). Performing data cleaning and preparation tasks to ensure data integrity and accuracy prior to analysis. Participating in the preparation of reports and documentation to support regulatory submissions and clinical study reports. Learning and applying industry standards, including ICH/GCP guidelines, to programming tasks to ensure compliance. Your Profile: Ba...
Posted 2 months ago
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