Senior Clinical Research Associate II - Sydney Trials

Senior Clinical Research Associate II - Sydney Trials

Sydney Full-Time 75600 - 92400 $ / year (est.) On-site
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At a Glance

  • Tasks: Manage clinical trials, ensuring quality and compliance while collaborating with a supportive team.
  • Company: Join ICON Clinical Research, a leader in innovative healthcare solutions.
  • Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
  • Other info: Dynamic environment with a focus on teamwork and career advancement.
  • Why this job: Make a real difference in healthcare by contributing to impactful clinical studies.
  • Qualifications: Healthcare degree and 18 months+ CRA experience required.

The predicted salary is between 75600 - 92400 $ per year.

ICON Clinical Research in Sydney, NSW, is seeking a CRA II/Senior CRA to join a dynamic, supportive team.

The position involves work on multiple studies across therapeutic areas, with responsibilities extending to study close-out and ongoing monitoring.

You will ensure adherence to SOPs and ICH-GCP, liaise with sites and stakeholders, and contribute to timelines and quality across trials.

A healthcare degree and 18 months+ CRA experience are required, with strong teamwork and a proactive

Senior Clinical Research Associate II - Sydney Trials 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 Senior Clinical Research Associate II - Sydney Trials

Clinical Research Experience
Knowledge of SOPs
Understanding of ICH-GCP
Study Monitoring
Study Close-Out Procedures
Stakeholder Liaison
Teamwork