Medpace is seeking a Clinical Research Monitor to perform qualification, initiation, monitoring and closeout visits at study sites in Australia, ensuring adherence to the approved protocol and GCP standards.
The role involves coordinating with site staff, verifying investigator qualifications, and ensuring proper documentation, safety reporting, and regulatory compliance throughout all monitoring activities.
Clinical Research Monitor — Site Compliance & Data Integrity 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.
