regulatory authorities regarding notifiable trial events
regulatory authorities regarding notifiable trial events Prepare for and manage participant visits and data Notify relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings
regulatory authorities regarding notifiable trial events Prepare for and manage participant visits and data Notify relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings
ever-changing environment
review the implementation and progress of site level implementation plans in conjunction with relevant implementation of clinical guidelines at a site level through on-site mentoring support and contribute RHI staff/stakeholders in sensitizing district level government authorities about programme activities appropriately resource, manage and mentor the district-level team
review the implementation and progress of site level implementation plans in conjunction with relevant implementation of clinical guidelines at a site level through on-site mentoring support and contribute RHI staff/stakeholders in sensitizing district level government authorities about programme activities appropriately resource, manage and mentor the district-level team Coach and train subordinates and team members
review the implementation and progress of site level implementation plans in conjunction with relevant implementation of clinical guidelines at a site level through on-site mentoring support and contribute RHI staff/stakeholders in sensitizing district level government authorities about programme activities appropriately resource, manage and mentor the district-level team Coach and train subordinates and team members