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Clinical Research Coordinator

2 months ago

Brisbane, Queensland, Australia ICON Full time

Job Summary:

As a Clinical Trial Assistant at ICON, you will play a vital role in supporting the success of our clinical research projects. This is an exciting opportunity to join a collaborative and growing team of clinical research professionals in Australia, focusing on developing vaccines.

Key Responsibilities:

  • Organize meetings, take minutes, and provide administrative support for investigator meetings
  • Track and update study metrics, ensuring timely and accurate reporting
  • Setup and maintain Trial Master File (TMF) and documents collection and quality check
  • Assist in study budget and expense management, oversight of site payment and vendor payment
  • Coordinate on drug supply plan, provision, and destruction process, trial equipment and materials plan and management
  • Coordinate vendors' activities, including printing, translation, and other vendors' management
  • Support the study team with distribution of site materials and equipment

Requirements:

  • Previous and solid CTA experience within the pharmaceutical or biotechnology industry or at investigative site
  • Basic knowledge and understanding of Essential Documents, CFR, and GCP/ICH
  • Proficiency with technological systems (Microsoft Office, TMF, CTMS)
  • Fundamental understanding of filing systems and organizational tools
  • BS/BA or equivalent preferred

About ICON:

At ICON, we are committed to providing a comprehensive and competitive total reward package that comprises an excellent level of base pay, a wide range of variable pay, and recognition programs. 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. We are an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment.