Study Coordinator
Cmax - A Division Of Idt Australia Limited
Adelaide, Australia
Coordination of clinical trials in healthy volunteers and patient populations, from ethics submission to study close-out and including subject/patient recruitment, participation in site initiation meetings, real-time supervision of confined study volunteers, recording of adverse events, reporting of serious adverse events, production of summary data for safety review, CRF data entry/transcription, data query resolution and sponsor/CRO liaison. Includes ADME, PK/PD, SAD/MAD, Safety & Efficacy trials..