Manage Project Team to ensure trial deliverables are on time, within budget and in appropriate quality, in compliance with applicable SOPs, ISO14155 / ICH-GCP and all applicable (local) regulations.Avania is a leading, full-service contract research organization focused on the management of clinical studies for medical devices, IVDs, biologics, and device-drug combination products internationally. Avania supports products from the first-in-human phase through the post-market phase with the same customized approach. When you need to advance your medical technology, it takes Avania.

• Coordinate study initiation, screening, on-study activities, and archiving.• Manage on-study conduct, dosing and recording of data in source notes• Liaise with Study Sponsors, Study Patients, Medical/Health Services • Monitoring patients’ safety and reporting appropriately• Experience in Haematology and Trial Centre

• Working in a highly pressurized and fast moving environment • Coordinate study initiation, recruitment, screening, on-study activities, and archiving.• Manage on-study conduct, dosing, sample processing and shipping, and recording of data in source notes• Liaise with Study Sponsors and Study Participants• Participate in the preparation and management of ethics submissions and approvals

• Assisting in clinical studies and the Clinical Research Coordinator• Assisting in laboratory processing• Data Entry• Performing clinical procedures such as blood sampling, measuring vital signs and electrocardiograms. • Working in a highly pressurized and fast moving environment