coordinating all clinical trial activities according to good clinical practice, the study protocol, and the site's trial to ensure protocol and GCP compliance
coordinating all clinical trial activities according to good clinical practice, the study protocol, and the site's 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
coordinating all clinical trial activities according to good clinical practice, the study protocol, and the site's 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
NGOs
and NGOs Ensure accountability, transparency, and good stewardship of DoH consumables, supported by the stakeholders Experience in data analysis and utilization Good understanding of quality improvement systems, monitoring
and NGOs Ensure accountability, transparency, and good stewardship of DoH consumables, supported by the stakeholders Experience in data analysis and utilization Good understanding of quality improvement systems, monitoring