Benefits
Flexible working conditions – Opportunity to work from home and versatile working hours
Visa sponsorship & transfer for qualified candidates already based in Australia
Competitive compensation
Competitive transportation allowance
Annual Merit increases
Variable Compensation Bonus Plan – Lucrative bonus calculated directly from the number of visits you do
Fast PACE – Accelerated, tailored training program based on your experience
No metric for minimum required days on site per month
Opportunity for cross‐functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager
Airline club allowance
Casual Dress Code
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company‐sponsored employee appreciation events
Employee health and wellness initiatives
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
Communicate with the medical site staff including coordinators, clinical research physicians and their site staff
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
Verify medical record and research source documentation against case report form data, inform the site staff of any entry errors,



ensure good documentation practices are adhered to and communicate protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements
Verify that the investigator is enrolling only eligible subjects
Review regulatory documents
Maintain investigational product/drug accountability and inventory
Review adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
Assess the clinical research site's patient recruitment and retention success and offer suggestions for improvement
Complete monitoring reports and follow‐up letters, which include providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
Qualifications
Bachelor's degree in a health or science related field
Prior 1 year of study coordinator/clinical research coordinator experience is preferred
Knowledgeable about Clinical Monitoring practices and procedures and able to represent the function in internal and external meetings (e.g., business development)
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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📌 Clinical Research Associate (Home-Based, Adelaide) (South Australia)
🏢 Medpace
📍 South Australia