- 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)
🏢 BVG India
📍 Chennai
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