Medpace in Melbourne seeks a clinical research monitor to conduct qualification, initiation, monitoring, and closeout visits across sites in compliance with the approved protocol. You will communicate with site staff, verify qualifications, training, facilities, and staff, and ensure accurate data reporting and regulatory compliance.
This role requires travel 60-80% nationwide (remote/virtual visits possible).
Clinical Research Associate — Site Monitoring & Travel in Melbourne employer: Medpace
Medpace is an exceptional employer, offering a dynamic work environment in Melbourne that fosters professional growth and development within the clinical research field. With a strong focus on employee well-being, competitive compensation, and flexible working arrangements, Medpace supports its team members in achieving their career aspirations while contributing to meaningful advancements in medical therapeutics. Join a globally recognized leader in the CRO industry, where your expertise will be valued and your contributions will make a real impact.
