)
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator site monitoring visits/audits or similar Manage procurement for the study Assist team members and support
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator site monitoring visits/audits or similar Manage procurement for the study Assist team members and support
adhering to relevant finance and procurement policies
adhering to relevant finance and procurement policies Analyse data to track progress towards targets management of multiple stakeholders Experience in data analysis and utilization Good understanding of quality reporting requirements Knowledge of clinical and data management and analysis Proactive, energetic team
adhering to relevant finance and procurement policies Analyse data to track progress towards targets management of multiple stakeholders Experience in data analysis and utilization Good understanding of quality reporting requirements Knowledge of clinical and data management and analysis Proactive, energetic team