Project Research Scientist - III(Medical)

Role & responsibilities

• 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.