Assist in planning, designing, and executing clinical trials involving Ayurvedic and/or integrative therapies
Participate in screening, recruiting, and monitoring clinical trial participants
Ensure accurate documentation of case reports and informed consent as per ICH-GCP guidelines
Collaborate with investigators, coordinators, and sponsors on trial-related activities
Review and ensure accuracy of medical and treatment data collected during trials
Monitor patient safety and report adverse events
Maintain regulatory and ethical compliance throughout the study
Support the team with literature reviews and protocol development
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