- Plan, coordinate, and monitor clinical trial activities.
- Ensure compliance with ICMR, GCP, and ethical guidelines.
- Supervise participant recruitment, screening, and follow-up.
- Maintain accurate clinical documentation and study records.
- Coordinate with investigators, laboratories, and regulatory bodies.
- Prepare technical reports, research publications, and progress updates.
- Ensure data quality, protocol adherence, and patient safety.
📌 Project Research Scientist - III(Medical) (Chennai)
🏢 BVG India
📍 Chennai
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