Benefits

- Adaptable working conditions – Opportunity to work from home and flexible 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
- Chance 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)
🏢 Medpace
📍 Adelaide