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medpace
Clinical Research Associate
Remote · Brisbane, Australia · Full time · Mid level
About the role
Conduct clinical research site visits and ensure compliance with protocols and regulations. Communicate with medical site staff and verify documentation accuracy.
What you’ll do
• Conduct qualification, initiation, monitoring, and closeout visits. • Communicate with medical site staff and coordinators. • Verify investigator qualifications and resources. • Review medical records and source documentation. • Complete monitoring reports and follow-up letters.
What you’ll bring
• Bachelor's degree in health or science field. • 2 years study coordinator or clinical research coordinator experience preferred. • Knowledge of clinical monitoring practices. • Ability to represent function in meetings. • Strong communication and documentation skills.
Life at medpace
Flexible working conditions with work from home and flexible hours. Visa sponsorship available. Competitive transportation allowance and bonus plan. Casual dress code and airline club allowance.
About medpace
Medpace is a full-service clinical contract research organization providing phase I-IV clinical development services globally. They focus on advancing medical therapeutics through clinical research excellence.