Job Summary :
We are currently seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team in Australia (Melbourne). This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities :

• Engage in clinical trial management on a day to day level
• Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy
• Compile and maintain project-specific status reports
• Update CTMS with study milestones, enrolment projections etc.
• Update eTMF and perform ongoing eTMF QC
• Support clinical trial manager to draft study plans and study specific guidance documents
• Manager site feasibility, site activation preparation and study supply managements
• Communicate with regional cross functional team, vendors and sponsor effectively

Qualifications :

• Bachelor’s degree in a health sciences field
• Maintain thorough knowledge of project and ability to coordinate/present at internal/external meetings and conference calls
• Excellent computer (word-processing, databases, Excel, Windows) and organizational skills

Medpace Overview :
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 its 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. Headquartered in Cincinnati, Ohio, employing more than 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 who face 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.

• Engage in clinical trial management on a day to day level
• Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy
• Compile and maintain project-specific status reports
• Update CTMS with study milestones, enrolment projections etc.
• Update eTMF and perform ongoing eTMF QC
• Support clinical trial manager to draft study plans and study specific guidance documents
• Manager site feasibility, site activation preparation and study supply managements
• Communicate with regional cross functional team, vendors and sponsor effectivel