Populations Programme team
Populations Programme team Regularly monitor and track site performance in relation to programme targets Actively participate in the Key Populations Programme's senior management team, providing support to recording of outputs to evaluate the impact of the programme Support the implementation of clinical guidelines Write, communicate and share work plans with all employees on site and review work plans when necessary Perform reporting, agreements & stakeholder engagements Coordinate with relevant Wits RHI staff/stakeholders in
Populations Programme team Regularly monitor and track site performance in relation to programme targets Actively participate in the Key Populations Programme's senior management team, providing support to recording of outputs to evaluate the impact of the programme Support the implementation of clinical guidelines Write, communicate and share work plans with all employees on site and review work plans when necessary Perform reporting, agreements & stakeholder engagements Coordinate with relevant Wits RHI staff/stakeholders in
i>The project manager/study coordinator is responsible for coordinating all clinical trial activities trial to ensure protocol and GCP compliance
job: The project manager/study coordinator is responsible for coordinating all clinical trial activities clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
job: The project manager/study coordinator is responsible for coordinating all clinical trial activities clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful
up to standard