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
managing complex disciplinary processes and investigations Experience in mediation, conflict resolution all disciplinary processes Conduct thorough investigations into disciplinary matters, gathering evidence interviewing relevant parties Prepare comprehensive investigation reports with clear findings and recommendations dialogues between parties Conduct thorough investigations into grievances, documenting all findings and and evidence Prepare detailed grievance investigation reports with clear conclusions and recommended
positive and constructive partnership with study Investigators and other site staff through constructive feedback
positive and constructive partnership with study Investigators and other site staff through constructive feedback
needed to the study coordinator and Principal investigator regarding clinical management of subjects Attend
needed to the study coordinator and Principal investigator regarding clinical management of subjects Attend