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Clinical Research Associate

4 weeks ago

Darwin, Northern Territory, Australia Pharmiweb Full time
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team in Oncology trials. As a CRA, you will be responsible for working on multiple trials, collaborating with country operations teams, and ensuring compliance with ICH-GCP guidelines and local regulatory standards.

Key Responsibilities
  • Perform Site Qualification Visits (SQVs) to assess site eligibility
  • Build strong relationships with site personnel to facilitate a smooth onboarding process
  • Ensure all activities adhere to ICH-GCP guidelines and local regulatory standards
  • Coordinate with country operations team to collect essential documents
  • Act as main point of contact for sites, study teams, and external stakeholders
Requirements
  • Bachelor's degree in Biological Sciences or equivalent
  • 2-3 years' experience in monitoring pharmaceutical industry clinical trials
  • Knowledge of several therapeutic areas
  • Ability to operate and use various systems and databases
  • Strong communication and influencing skills
What We Offer

We offer a competitive salary, annual leave entitlements, health insurance, and a range of other benefits to support your well-being and work-life balance.

At ICON, diversity, inclusion, and belonging are fundamental to our culture and values. We are committed to providing an inclusive and accessible environment for all candidates.