(Clinical Research Cordinator - Clinical trail Phase III )• Preparing site for the study • Compliance of study activity to protocol, GCP, Site SOP, Applicable regulatory requirement• Screening patient for the study• Enrolling patient in the study• Randomization• Dispensing of Study drug and accountability of study drug• Processing and shipping lab specimen• Scheduling subject visit• Assisting PI in all of his work• Maintaining source data • Maintaining study-specific supplies• Completion of CRF for PI review• Checking of CRF with source document and other related things against each other• Communicating with all party involved in the study (IEC, Sponsor, Central lab, etc)• Regulatory submission of document received at the site• Recording and processing adverse event/ Serious adverse event• Facilitate monitoring and auditing

• Project Management• Preparation of Site for study• Preparation of Study Master File• Monitoring of study activity for compliance of protocol, Sop’s and GCP• Screening process• Informed consent process• Managing and maintaining study forms supplies, equipment, etc• Drug administration and accountability• Assisting principle investigator, medical officer, phlebotomist • Compilation of source data • Completion of CRF for PI review• Checking of CRF with source document and other related things against each other• Recording and processing adverse event/ Serious adverse event• Faciliate monitoring and auditing • Assisting in Preparation of final integrated study report.• Preparation of Informed Consent Form• Preparation of Case Report Form• Preparation and reviewing of SOP