What We Offer
* Flexible working conditions, including the opportunity to work from home and flexible working hours.
* Visa sponsorship and transfer for qualified candidates already based in Australia.
* A competitive transportation allowance.
* Annual merit increases.
* A variable compensation bonus plan, offering a lucrative bonus calculated directly from the number of visits conducted.
* A fast-paced training program tailored to individual experience (Fast PACE).
* No minimum requirement for days spent on site per month.
* Opportunities for cross-functional and CRA leadership positions, such as Lead CRA, CRA Manager, Clinical Trial Manager.
* An airline club allowance.
* A casual dress code.
Responsibilities
* Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with approved protocols.
* Communicate with medical site staff, including coordinators, clinical research physicians, and their site personnel.
* Verify investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff.
* Verify medical record and research source documentation against case report form data, ensuring good documentation practices are being followed and communicating protocol deviations appropriately according to SOPs, GCP, and applicable regulatory requirements.
* Ensure investigators are enrolling only eligible subjects.
* Review regulatory documents.
* Verify investigational product/drug accountability and inventory.
* Review adverse events, serious adverse events, concomitant medications, and corresponding illnesses to confirm accurate data reporting according to the protocol.
* Evaluate the clinical research site's patient recruitment and retention success and suggest improvements.
* Complete monitoring reports and follow-up letters, providing summaries of significant findings, deviations, deficiencies, and recommended actions to secure compliance.
Qualifications
* Bachelor's degree in a health or science-related field, along with at least 1.5 to 5 years of experience in clinical monitoring.
* Knowledge of Clinical Monitoring practices and procedures, representing the function in internal and external meetings.
About Us
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective diseases. Headquartered in Cincinnati, Ohio, we employ over 5,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families facing hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Medpace Perks
* A flexible work environment.
* A competitive compensation and benefits package.
* A competitive PTO package.
* Structured career paths with opportunities for professional growth.
* Company-sponsored employee appreciation events.
* Employee health and wellness initiatives.
Awards
* Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
* Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.