09 Sep
|
BVG India
|
Chennai
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.
📌 Project Research Scientist Iii Medical Chennai
🏢 BVG India
📍 Chennai