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Clinical Research Associate

2 months ago

Sydney, New South Wales, Australia ICON Full time
About the Role

We are seeking an experienced Clinical Research Associate to join our team at ICON, a world-leading pharmaceutical company. As a key member of our study team, you will be responsible for performing all aspects of CRA duties, from site selection to database lock.

Key Responsibilities
  • Perform site selection, site initiation, routine monitoring visits, and close-out visits (on-site and remote)
  • Oversee all aspects of study site management to ensure high-quality data and consistently low query levels
  • Collaborate with our client's study team and have a dedicated ICON functional manager to support you
Requirements
  • Degree in Pharmacy or a related field
  • 2+ years of prior monitoring experience with global trials within a CRO or pharmaceutical company
  • Excellent written and verbal communication skills
  • Strong knowledge of international guidelines ICH-GCP and local regulations
  • Flexibility to travel and work from the sponsor office for around 3 days/week (if not traveling)
About ICON

At ICON, we value diversity, inclusion, and belonging. Our rich diversity makes us more innovative, and we're dedicated to providing an inclusive and accessible environment for all candidates. We're committed to providing a workplace free of discrimination and harassment.

We offer a range of benefits, including competitive salary, annual leave entitlements, health insurance, retirement planning, and more. Visit our careers website to learn more about the benefits of working at ICON.