Clinical Research Associate II

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Facilitate site budgets and contract negotiations
• Monitor trial progress on the country level
• Be responsible for site communication and management
• Serve as a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support the regulatory team in preparing documents for study submissions
• Manage the clinical aspects of full-service global projects in Australia
• Ensure timelines, targets and clinical research standards
• Build and maintain relationships with clinical sites and investigators
• Focus on subjects’ rights, safety and well-being and quality of data compliance

• College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
• At least 2 years of independent on-site monitoring experience in Australia
• Experience in all types of monitoring visits in Phase II and/or III
• Experience in Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus
• Full working proficiency in English
• PC skills to be able to work with MS Word, Excel and PowerPoint
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• Ability to travel

• Competitive salary
• Hybrid work arrangement: 2 days flexi and 3 days in office
• Onsite Gym access
• Additional 5 days of wellness leave
• Development and learning opportunities
• Chance to make a real impact in a meaningful industry
• Continuous support from global peers
• On-the-job learning experiences
• Formal development programs
• Variety of opportunities to continue to grow throughout your career