resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Communicate with with all relevant SOPs Communicate well with investigators regarding participant welfare while on study and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings, SIV, and any other key meetings to manage the study Manage site monitoring visits/audits or similar Manage procurement for the study Assist
resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Communicate with with all relevant SOPs Communicate well with investigators regarding participant welfare while on study and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings, SIV, and any other key meetings to manage the study Manage site monitoring visits/audits or similar Manage procurement for the study Assist
resolve protocol queries and missing data with Investigators and Clinical Trials Assistants
SOP
Support in the preparation of monitoring visits, audits, site inspections, and similar Support data clean-up
Support in the preparation of monitoring visits, audits, site inspections, and similar Support data clean-up
prioritize information system needs
prioritize information system needs Conduct data audits and routine data quality assessments in different
prioritize information system needs Conduct data audits and routine data quality assessments in different