Clinical Trial Site Coordinator: Monitoring & Compliance in Sydney

Clinical Trial Site Coordinator: Monitoring & Compliance in Sydney

Sydney Full-Time 45000 - 55000 $ / year (est.) On-site
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At a Glance

  • Tasks: Support clinical trial site management and ensure compliance with protocols.
  • Company: Join ICON Strategic Solutions, a leader in clinical research.
  • Benefits: Gain valuable experience, travel opportunities, and work with global experts.
  • Other info: Exciting career growth potential in the clinical research field.
  • Why this job: Make a difference in healthcare while developing your skills in a dynamic environment.
  • Qualifications: Strong attention to detail and ability to work in cross-functional teams.

The predicted salary is between 45000 - 55000 $ per year.

ICON Strategic Solutions is seeking a SMA I to support clinical trial site management and monitoring activities.

You will assist in ensuring protocol adherence and GCP compliance while coordinating with cross-functional teams to maintain high operational standards.

The role emphasizes site documentation, data entry, and preparation of monitoring reports.

Involves travel (about 25%) and working within ICON's sponsor-dedicated model leveraging global expertise.

Clinical Trial Site Coordinator: Monitoring & Compliance in Sydney employer: ICON Clinical Research

At ICON Strategic Solutions, we pride ourselves on being an exceptional employer, offering a supportive and collaborative work environment for Clinical Research Associates in Perth, Australia. With a strong focus on employee well-being, we provide competitive benefits, including flexible leave options, comprehensive health insurance, and a commitment to professional development, ensuring that our team members thrive both personally and professionally while contributing to groundbreaking medical advancements.

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Contact Details:

ICON Clinical Research Recruitment Team

We think you need these skills to ace Clinical Trial Site Coordinator: Monitoring & Compliance in Sydney

Clinical Trial Management
Good Clinical Practice (GCP) Compliance
Protocol Adherence
Site Documentation
Data Entry
Monitoring Reports Preparation
Cross-Functional Team Coordination