across all sites, collating and reviewing hazards and risks. Arrange adequate First Aid across sites. Respond all safety documents once a year. Attending all site safety meetings and creating minutes of all meetings
across all sites, collating and reviewing hazards and risks. Arrange adequate First Aid across sites.
Respond
safety documents once a year.
Attending all site safety meetings and creating minutes of all meetings
across all sites, collating and reviewing hazards and risks. Arrange adequate First Aid across sites. Respond all safety documents once a year. Attending all site safety meetings and creating minutes of all meetings
recruitment and data collection at the allocated study sites
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
guidelines and legal requirements.
Academic Hospital (Soweto – Johannesburg) and field sites as per study requirements
Key
ent the study protocol and procedures at study sites consistently and accurately, as directed
Academic Hospital (Soweto – Johannesburg) and field sites as per study requirements Key performance areas: Implement the study protocol and procedures at study sites consistently and accurately, as directed Conduct
Academic Hospital (Soweto – Johannesburg) and field sites as per study requirements Key performance areas: Implement the study protocol and procedures at study sites consistently and accurately, as directed Conduct