Clinical Research Associate II
HybridSydney, New South Wales, Australia
Job Summary
Conduct onsite monitoring visits, perform CRF review, source document verification, and query resolution. Manage study startup, facilitate site budgets, and negotiate contracts. Monitor trial progress at the country level, build relationships with clinical sites, and serve as a point of contact for vendors. Communicate with internal teams regarding study progress and participate in feasibility research. Support regulatory teams in preparing documents for study submissions. This role requires at least two years of independent on-site monitoring experience in Australia and proficiency in English. Located in Macquarie Park, NSW, the position offers a hybrid arrangement with competitive salary and wellness benefits.
Required Qualifications
- 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
- 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
Desired Qualifications
- Experience in feasibility assessment and study set-up process is preferable
- Experience in Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus
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