Clinical Trial Monitoring, data integrity, ICH-GCP guidelines, protocol compliance, Data Review

Source document verification, Query Resolution, On-site monitoring, Feasibility research, Contract Negotiation, CRF review

Investigational Product accountability, ICH GCP Guidelines, Clinical Monitoring Plan, Site monitoring and management

clinical site monitoring , clinical site management , Ms Office, Clinical IT applications, Clinical Study Management, Good Documentation Practices, Adverse Event Reporting, Regulatory Compliance, Data Analysis

Study site management, Clinical Trial Management, Data Review, Patient Safety, On-site monitoring

Clinical Trial Management, Site Management, Data Review, ICH-GCP