submission to the study coordinator/leadership team Assist in patient recruitment, screening, enrolment, and according to protocol requirements as and when required Assist with stock-take for the project, ensuring stock maintained and low stock is flagged for procurement Assist the team with ad hoc assignments and duties as
submission to the study coordinator/leadership team Assist in patient recruitment, screening, enrolment, and according to protocol requirements as and when required Assist with stock-take for the project, ensuring stock maintained and low stock is flagged for procurement Assist the team with ad hoc assignments and duties as
compliance to OHS Act and applicable regulations bu assisting, giving advise, and enforcing HSE issues related root causes and develop corrective action plans Assist in the development of emergency response plans employees to promote a culture of safety and accountability Stay informed about changes in health and safety
compliance to OHS Act and applicable regulations bu assisting, giving advise, and enforcing HSE issues related root causes and develop corrective action plans Assist in the development of emergency response plans employees to promote a culture of safety and accountability Stay informed about changes in health and safety
monitoring reviews Assist in the completion of corrective action for monitoring reviews Assist/ensure completion documentation available and up to date across all studies Assist with the review and revision of standard operating error trends are identified Take ownership and accountability for tasks and demonstrate effective self-management
monitoring reviews Assist in the completion of corrective action for monitoring reviews Assist/ensure completion documentation available and up to date across all studies Assist with the review and revision of standard operating error trends are identified Take ownership and accountability for tasks and demonstrate effective self-management
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 attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
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 attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
surveillance inspections. Technical Quality: 5. Assist with technical quality specification reviews and measuring, and reporting on various quality data. 8. Assist with quality compliance audits and assessments
report to the Head: Corporate Actuarial and will assist with the following: Calculation and management