Syneos Health, Inc. in Australia is seeking a Clinical Research Associate I for Real World Late Phase studies. The role supports site qualification, initiation, and monitoring visits, ensuring regulatory compliance and data integrity.
Responsibilities include source data verification, IP handling, and ISF/TMF reconciliation, with collaboration across sponsor teams. Travel up to 75% is required, with in office or remote activities as applicable.
#J-18808-Ljbffr
📌 Site Monitoring Pro for Clinical Trials (Adelaide)
🏢 Syneos Health
📍 Adelaide
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.