Clinical research coordinatorCommunication to the sponsor related to clinical activitiesAssist investigator to conduct study as per protocol, ICH-GCP and applicable RA.Initial assessment of inclusion exclusion criteriaPatient registration, randomization and schedule patient visit as per schedule of assessmentPatient screening and accountabilityEDC, CRF and e-CRF filling and query resolution Drug dispensing and accountabilitySite selection, site initiation visit… Show more Clinical research coordinatorCommunication to the sponsor related to clinical activitiesAssist investigator to conduct study as per protocol, ICH-GCP and applicable RA.Initial assessment of inclusion exclusion criteriaPatient registration, randomization and schedule patient visit as per schedule of assessmentPatient screening and accountabilityEDC, CRF and e-CRF filling and query resolution Drug dispensing and accountabilitySite selection, site initiation visit to site close out visit and SOP preparationCapturing, notifying and reporting AE/SAE/SUSAR to Ethics committeeCIOMS preparation and reporting to ECCompleting and ensuring the quality of CRFMaintaining Site Master File Show less