Role & Responsibility Be responsible for the delivery of the studies at allocated sites and works in close collaboration with other CRAs and the local study team to ensure that quality commitments are achieved in a timely and efficient manner. Conduct site feasibility assessment. Contribute to the selection of potential investigators and leading investigator. Contribute to national Investigator meeting. Perform source data verification. Proactively identify study-related issues and escalates as appropriate. Complete monitoring visit reports within required timelines. Document the issues and follow up with sites until it is resolved. Ensure accurate and timely reporting of Serious Adverse Events. Work with data management to ensure quality of the study data. Ensure data query resolution. Prepare for activities associated with audit and regulatory inspection at responsible sites and/country in liaison with local study team lead and QA. Ensure compliance with company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). Requirement Pharmacy & Medical Related Master Good medical knowledge and basic understanding of the drug development process. Fluent knowledge of spoken, read and written English. Team oriented and flexible. Ability to manage & prioritize multiple tasks with conflicting deadlines ability to work in an environment of remote collaborators Meticulous and detail-oriented