• Clinical Trial preparation involving planning, development and evaluation of patient information and informed consent forms. • Regulatory/Ethical submission and communication with relevant authorities. • Determining eligibility based on inclusion & exclusion criteria. • Enrollment and follow up of recruited subjects to minimize dropouts. • Performing the trials according to the protocol and GCP. • Maintenance of investigator files at the site. • Management of Trials at the site. • Creates and maintains appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. • CRF completion and submission, and data query generation and resolution. • Obtain and maintenance essential documentation in compliance with ICH­GCP and local regulations both in trial master file and Investigators Site File (ISF).