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 of Serious Adverse Events or Events of Medical Importance as per protocol requirements. Quality control
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 of Serious Adverse Events or Events of Medical Importance as per protocol requirements. Quality control
agreements & stakeholder engagements
reporting, agreements & stakeholder engagements Coordinate with relevant Wits RHI staff/stakeholders in sub-partners, and other district stakeholders Coordinate with other NGOs, private sector players and internal synergies are achieved to avoid duplication of effort Coordinate closely with senior management and the relevant
reporting, agreements & stakeholder engagements Coordinate with relevant Wits RHI staff/stakeholders in sub-partners, and other district stakeholders Coordinate with other NGOs, private sector players and internal synergies are achieved to avoid duplication of effort Coordinate closely with senior management and the relevant
up to standard