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
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
retention samples in the QC lab • Assist with investigating of internal and external NCRs • Assist with