Role & responsibilities
Design and develop statistical analysis plans for clinical trials.
Perform biostatistical analysis and interpretation of clinical data.
Manage clinical trial databases and ensure data quality.
Prepare statistical reports, tables, and study results.
Support protocol development and sample size calculations.
Coordinate with investigators and research teams for data management.
Ensure compliance with GCP, ICMR, and regulatory guidelines.
📌 Project Research Scientist Iii Non Medical Chennai (India)
🏢 BVG India
📍 India
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