start-up, conduct, and close-out
study start-up, conduct, and close-out Manage regulatory updates throughout the study (New ICFs, Protocol Assistants Communicate with CRO, Sponsor, and regulatory authorities regarding notifiable trial events
study start-up, conduct, and close-out Manage regulatory updates throughout the study (New ICFs, Protocol Assistants Communicate with CRO, Sponsor, and regulatory authorities regarding notifiable trial events
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
responsible for customer management, support, reporting and involved in all projects at the customer<