Clinical Research Associate II
At ICON, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
Responsibilities
* Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits (on-site and remote) and database lock.
* You will be fully embedded in our client's study team and have a dedicated ICON functional manager to support you.
* Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports.
Qualifications
* Tertiary degree qualified in health/science.
* At least 2 years local CRA experience in CRO/pharma is required and you ideally have previous experience monitoring oncology trials.
* You will be able to commit to travelling to sites interstate on occasion.
* Although continuous support will be provided, due to the remote nature of the role, you must be confident working autonomously to ensure delivery of expectations.
What ICON can offer you
* Variety of annual leave entitlements.
* A range of health insurance offerings to suit you and your family's needs.
* Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead.
* Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
* Life assurance.
* Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.