Tejashree Khairnar

· Patient recruitment for study with protocol compliance.

· Management and supervision of accuracy of study materials, logistics, and storage.

· Supporting Research Coordinator and Principal Investigator to oversee the management and reporting of data

· Maintaining and managing access to study database and systems for all study personnel

· Compilation and review documentation required for Good Clinical Practice and/or as required from the study sponsor.

· Overseeing multiple trials at the site.

· Clinical Data Management with various softwares. Trial Master, REDCap, ROME, EPIC.

• Monitored Compliance with study protocols, SOP, ICH-GCP, and local Regulations
• IB, Protocol, CRF, Informed Consent design, IRB approval, SSU
• Developed Case Report Form and Informed Consent Form
• Clinical Data Management.

• Established and maintained relationships with fellow volunteers and organizational stakeholders.

• Kept patient information confidential and respected patients rights to privacy
• Treated patients on emergency basis to repair teeth injuries, prescribed medications, and performed minor surgical procedures
• Treated, supported and cared for 40 patients per day on average by efficiently focusing on individual patients.