As a Clinical Research Coordinator I have experience in multicentric studies. Like:•Coordinates approval of new study agreements and contracts.•Coordinates with PIs and department to help ensure that clinical research and related activities are performed in accordance with protocol, SOP, GCP and applicable regulatory requirement•Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.Assists in preparation of all documents related to the informed consent process.•Skilled In--Good Clinical Practice. -Electric Data Capture & Paper CRF-Patient Tracking as per schedule Visit.-Coordinates participant tests and procedures.-Dispensed Medicine As per IWRS.-Maintains study timelines.-Visit specific activities.-Collects specimens & Send to the Central Lab.-Safety guidelines and reporting timelines as per the protocol.-Maintains subject screening logs and protocol deviation logs.•Assists the Principal Investigator in submission of accurate and timely closeout documents to the sponsoring agency in accordance with university and sponsoring agency policies and procedures.