job:
purpose of the job: The project manager/study coordinator is responsible for coordinating all clinical trial requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings
purpose of the job: The project manager/study coordinator is responsible for coordinating all clinical trial requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator meetings
review the implementation and progress of site level implementation plans in conjunction with relevant providing support to all activities and special projects
review the implementation and progress of site level implementation plans in conjunction with relevant providing support to all activities and special projects Support the development of effective outreach implementation of clinical guidelines at a site level through on-site mentoring support and contribute engagements Coordinate with relevant Wits RHI staff/stakeholders in sensitizing district level government sub-partners, and other district stakeholders Coordinate with other NGOs, private sector players and internal
review the implementation and progress of site level implementation plans in conjunction with relevant providing support to all activities and special projects Support the development of effective outreach implementation of clinical guidelines at a site level through on-site mentoring support and contribute engagements Coordinate with relevant Wits RHI staff/stakeholders in sensitizing district level government sub-partners, and other district stakeholders Coordinate with other NGOs, private sector players and internal
management, support, reporting and involved in all projects at the customer
Location:
adaptable