)
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants 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 independent decision-making Ability to prioritize own workload, take initiative (pro-active), and work Overtime and traveling will be required from time to time Light physical activity is required TO APPLY:
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials Assistants 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 independent decision-making Ability to prioritize own workload, take initiative (pro-active), and work Overtime and traveling will be required from time to time Light physical activity is required TO APPLY:
and training plans
finance and procurement policies
relevant finance and procurement policies Analyse data to track progress towards targets and optimize implementation 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
relevant finance and procurement policies Analyse data to track progress towards targets and optimize implementation 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