trial to ensure protocol and GCP compliance
compliance Assist study team with efficient study start-up, conduct, and close-out Manage regulatory updates Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory authorities regarding 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 attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
compliance Assist study team with efficient study start-up, conduct, and close-out Manage regulatory updates Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory authorities regarding 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 attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
responsible for customer management, support, reporting and involved in all projects at the customer< up to standard
associated with accurate clinical record keeping and reporting including patient records and confidentiality
associated with accurate clinical record keeping and reporting including patient records and confidentiality of DoH consumables, supported by the required reporting, agreements & stakeholder engagements Coordinate Experience working with donor funded programmes and reporting requirements Knowledge of clinical and data management
associated with accurate clinical record keeping and reporting including patient records and confidentiality of DoH consumables, supported by the required reporting, agreements & stakeholder engagements Coordinate Experience working with donor funded programmes and reporting requirements Knowledge of clinical and data management