As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career whilst truly making an impact.
**What you will be doing**:
- Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock.
- You will be embedded in our client's study team and have a dedicated ICON line manager to support you
- Joining ICON's Strategic Solutions division, the global leader in fucntional service provision
- Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports
- Fully home based with travel to sites as required
**You are**:
- Degree in Pharmacy or any related course.
- 2+ years prior monitoring experience with global trials.
- Excellent communication skills
- Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP, good knowledge of local regulations.
- Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
**Why ICON?**
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your career development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
📌 Clinical Research Associate
🏢 Icon
📍 Brisbane