To provide clinical support for projects according to Standard Operating Procedures, ICH Guidelines and GCP. - To develop and/or maintain tracking systems for clinical projects. - Responsible for all aspects of study site monitoring with or without direct supervision (as per the training status of the CRA I MEA). This includes remote and/or onsite conduct of pre-study visits, site initiation visits, routine monitoring visits and close-out visits of clinical sites. - Conduct site management acti…