I want to do Clinical Trials. Iam Medica Doctor, PhD. Experienced Senior CRA with a demonstrated history of working in the pharmaceuticals industry. I have had advanced for the full monitoring of activities: feasibility, site selection and recruitment, collection of regulatory packages, Ethics and Regulatory submissions. site initiation, monitoring and close out.logistic and regulatory issues related to import and delivery of IMP and other clinical trial supplies to the sites; SD and eCRF verification, AE/ SAE managment, query resolution and archiving. I've experiencee with several Audit and client visits, without any major and critical findings. Strong information technology professional with a Doctor of Philosophy - PhD focused in medical from TSMU.