distributing study information (as applicable) at study sites and/or in communities Address potential participants at identified study sites Conduct Informed Consent discussion according to site ICF SOP Conduct surveys Support data capture and data quality control on sites Engage with stakeholders and community members to provide information about the study Liaise with the site manager, stakeholders and community members to identify has relevant study materials (HREC approved) on site Identify missing data, inconsistencies and/or errors
distributing study information (as applicable) at study sites and/or in communities Address potential participants at identified study sites Conduct Informed Consent discussion according to site ICF SOP Conduct surveys Support data capture and data quality control on sites Engage with stakeholders and community members to provide information about the study Liaise with the site manager, stakeholders and community members to identify has relevant study materials (HREC approved) on site Identify missing data, inconsistencies and/or errors
distributing study information (as applicable) at study sites and/or in communities
recruitment and data collection at the allocated study sites Where appropriate, they will also contribute towards participants about the OptiMVacc study at study sites Conduct screening interviews with potential participants Conduct Informed Consent discussion according to site ICF SOP Conduct surveys and/or qualitative interviews
recruitment and data collection at the allocated study sites Where appropriate, they will also contribute towards participants about the OptiMVacc study at study sites Conduct screening interviews with potential participants Conduct Informed Consent discussion according to site ICF SOP Conduct surveys and/or qualitative interviews
recruitment and data collection at the allocated study sites