Clinical Research Associate II

About the role

Monitors clinical trial sites and keeps studies on track across several therapeutic areas. Acts as the main link between the sponsor side and investigators, protecting participants and data quality.

What you will do

• Carry out and document every kind of on-site monitoring visit
• Take part in study start-up activities
• Review case report forms, verify source documents and resolve queries
• Help negotiate site budgets and contracts
• Track trial progress at country level and manage site communication
• Liaise with internal teams and vendors, and support feasibility and regulatory submissions

What they look for

• A degree in life sciences, pharmacy or nursing, or equivalent training and experience
• At least two years of independent on-site monitoring in Australia
• Experience with all monitoring visit types in phase II or III trials
• Full professional fluency in English
• Comfort with MS Word, Excel and PowerPoint
• Planning and multitasking skills, teamwork, communication and problem solving, plus willingness to travel

Nice to have

• Background in inflammatory bowel disease, oncology or infectious diseases

Benefits

• Competitive salary
• Hybrid schedule with two flexible days and three office days
• Onsite gym access
• Five extra wellness days
• Learning and development opportunities